K103456 · Trek Diagnostic Systems · LIE · Jun 22, 2011 · Microbiology
Device Facts
Record ID
K103456
Device Name
THE SENSITITRE AIM
Applicant
Trek Diagnostic Systems
Product Code
LIE · Microbiology
Decision Date
Jun 22, 2011
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 866.1640
Device Class
Class 2
Indications for Use
The Sensititre® AIM™ is intended for use with the Sensititre® MIC or BP Susceptibility Test System. The Sensititre® AIM™ is an instrument used to inoculate Sensititre® MIC or BP Susceptibility plates. The Sensititre MIC or Breakpoint Susceptibility System is an in vitro diagnostic product for clinical susceptibility testing of gram positive and fastidious organisms comprising of Haemophilus influenzae, Streptococci pneumoniae, other Streptococci spp. and Candida spp.
Device Story
Sensititre AIM™ is a microprocessor-controlled, bench-top automated pipette system for inoculating 96-well micro-titre plates used in antimicrobial susceptibility testing (AST). User prepares bacterial suspension; affixes disposable dosehead to glass tube; places tube into pump assembly. User selects well dose volume (50μl multiples) via graphical display. Instrument dispenses inoculum into plates. Stand-alone device; no sample tracking or external connectivity. Healthcare providers use output (MIC plates) to determine bacterial susceptibility to antimicrobial agents, aiding clinical treatment decisions. Benefits include standardized, automated inoculation compared to manual methods.
Clinical Evidence
No clinical data provided; device is an automated laboratory instrument for plate inoculation.
Technological Characteristics
Microprocessor-controlled pump assembly; dispenses 50µl multiples; utilizes disposable doseheads; designed for 96-well microtiter plates; standalone laboratory instrument.
Indications for Use
Indicated for clinical susceptibility testing of gram-positive and fastidious organisms (Haemophilus influenzae, Streptococci pneumoniae, other Streptococci spp., and Candida spp.) using the Sensititre MIC or BP Susceptibility Test System.
Regulatory Classification
Identification
An antimicrobial susceptibility test powder is a device that consists of an antimicrobial drug powder packaged in vials in specified amounts and intended for use in clinical laboratories for determining in vitro susceptibility of bacterial pathogens to these therapeutic agents. Test results are used to determine the antimicrobial agent of choice in the treatment of bacterial diseases.
Submission Summary (Full Text)
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# 510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION DECISION SUMMARY ASSAY AND INSTRUMENT COMBINATION TEMPLATE
A. 510(k) Number:
k103456
B. Purpose for Submission:
To obtain substantial equivalence for the Autoinoculator 2, AIM™ inoculation system compared to the existing Autoinoculator I.
C. Measurand:
Antimicrobial susceptibility testing of Gram positive organisms, Streptococci, H. influenzae, and C. albicans on the Sensititre panels inoculated with AIM.
D. Type of Test:
Quantitative Antimicrobial Susceptibility Test (AST), growth based fluorescence. The minimum inhibitory concentration (MIC) is determined manually based on visual detection of growth or by the aid of a manual mirror viewer, an AutoReader or on the VIZION.
E. Applicant:
Trek Diagnostic Systems.
F. Proprietary and Established Names:
Sensititre 18 – 24 hour Susceptibility MIC Plates
Sensititre AIM™ inoculation system
G. Regulatory Information:
1. Regulation section:
21 CFR 866.1640 Antimicrobial Susceptibility Test Powder
2. Classification:
Class II
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3. Product code:
LIE-Reagents/Device, Inoculum Calibration
JWY-Manual readings of AST testing of >16 hour incubation
LRG-Automated readings of AST of >16 hrs incubation
4. Panel:
83, Microbiology
H. Intended Use:
1. Intended use(s):
The Sensititre® AIM™ is intended for use with the Sensititre® MIC or BP Susceptibility Test System. The Sensititre® AIM™ is an instrument used to inoculate Sensititre® MIC or BP Susceptibility plates.
The Sensititre MIC and Breakpoint Susceptibility system is an in vitro diagnostic product for clinical susceptibility testing of Gram positive organisms, Streptococci, H. influenzae, and C. albicans.
1. Indication(s) for use:
The Sensititre® AIM™ is intended for use with the Sensititre® MIC or BP Susceptibility Test System. The Sensititre® AIM™ is an instrument used to inoculate Sensititre MIC or BP Susceptibility plates.
The Sensititre MIC or Breakpoint Susceptibility System is an in vitro diagnostic product for clinical susceptibility testing of Gram positive organisms, Streptococcus pneumoniae, other Streptococcus spp., H. influenzae, and Candida spp.
This 510(k) is for the addition of: "AIM™"
The Sensititre AIM™ is a microprocessor controlled instrument that delivers inoculum in 50μl multiples to the Sensititre 96 well micro-titre plate. The user prepares the inoculum suspension in accordance with the package inert. A Sensititre disposable dosehead is affixed to the glass tube containing the final inoculum density which is placed into the AIM's pump assembly. The inoculum is then dispensed into the microtitre plates.
3. Special conditions for use statement(s):
Prescription use only.
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4. Special instrument requirements:
The Sensititre AutoReader
The Sensititre viewer, VIZION
The Sensititre Autoinoculator 2, AIM™ instrument
I. Device Description:
The Sensititre Autoinoculator 2, AIM™ instrument is an automated pipette system for the delivery of user prepared inoculated media in multiples of 50 and 100 µl into the Sensititre 96 well antimicrobial susceptibility plate.
The AIM™ is a bench-top instrument which dispenses bacterial suspension (inoculum) into a 96-well plate (MIC panel). The instrument has a display which presents options to the user graphically. The user may then select the well dose volume (a multiple of 50 µl) specific to each panel section. Different panel sections may be dosed differently. After selection of these parameters, the user loads the inoculum tube, a suitable panel and then starts the dosing cycle.
The AIM™ is a stand-alone device and requires no connections to other equipment in normal use. It currently provides no support for sample tracking.
J. Substantial Equivalence Information:
1. Predicate device name(s):
Autoinoculator I
2. Predicate K number(s):
k081063
3. Comparison with predicate:
| Similarities | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Intended Use | Delivery of prepared inoculum media in multiples of 50 µl into 96 microplate wells | Same |
| Inoculation and test organism | Isolated colonies from culture are used to prepare the inoculum | Same |
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| Similarities | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Dosing system /Technology | Automated pipette system using TREK dosehead consumables | Same |
| Well indexing method | Microplate wells are indexed beneath the dose head | Same |
| Calibration method | System is calibrated by weighing dosed plates | Same |
| Type of test | Automated or manual | Same |
| Differences | | |
| --- | --- | --- |
| Item | Device | Predicate |
| Size | 250 mm wide/350 mm deep | 413 mm wide/464 mm deep |
| Cycle speed | Between 27 and 35 seconds | 35 seconds |
| Dose head drive system | Single stepper motor articulating mechanically slaved rotation and thrusting movements of dose head drive spigot | Two stepper motors. First stepper motor articulating rotation movement of dose head drive spigot. Second stepper motor articulating thrusting movements of dose head drive spigot |
| User interface | Single line LED display with keypad | Touch screen display with icon driven menu system |
K. Standard/Guidance Document Referenced (if applicable):
1. Class II Special Controls Guidance Document: Antimicrobial Susceptibility Test (AST) Systems; Guidance for Industry and FDA
http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm071462.pdf
2. Clinical and Laboratory Standards Institute (CLSI). Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically, Approved Standard -8th Edition, Document M7-A8.
3. CLSI. Performance Standards for Antimicrobial Susceptibility Testing – 19th Informational Supplement, Document M100-S19.
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L. Test Principle:
Sensititre susceptibility plates are multi-well plastic microtiter plates that contain doubling dilutions of antibacterial agents. Each plate is dosed with antimicrobial agents at appropriate dilutions. Results can be read manually by visual reading of growth or automatically on an AutoReader using fluorescence. The Sensititre AutoReader system utilizes fluorescence technology which involves the detection of bacterial growth by monitoring the activity of specific surface enzymes produced by the test organism. Growth is determined by generating a fluorescent product from a non-fluorescent (fluorogenic) substrate. The substrate can be added to the inoculum broth and dispensed into the test plates at the same time as the test organism or the plates can be prepared with the substrate already added to the plate. The non-fluorescent substrate is prepared by conjugating a fluorescent compound to the specific enzyme substrates with a bond, which prevents fluorescence (i.e. the fluorophore is quenched in this state). Enzymatic action of the bacterial surface enzymes on the specific substrates cleaves this bond releasing the fluorophore which is now capable of fluorescence. The amount of fluorescence detected is directly related to the activity of the bacterial surface enzymes and, therefore, to bacterial growth.
M. Performance Characteristics (if/when applicable):
1. Analytical performance:
a. Precision/Reproducibility:
A reproducibility study was conducted at three study sites. For each group of organisms, twenty five isolates were inoculated using the AIM and tested at each site. The panels used included the antimicrobial agents as representatives of the various classes. These panels were tested one time at each of the three sites and results were read by both the AutoReader and the VIZION. The reproducibility of MIC tests was performed using Sensititre plates read on the VIZION, AutoReader, and/or mirror as follows
Gram positive - Read on AutoReader and VIZION
Streptococcus spp. - Read on AutoReader and VIZION
Haemophilus spp. - Read on the VIZION
Candida spp. - Read on manual mirror
Reproducibility was calculated as the percent of combined results were within +/- one doubling dilution of the mode MIC value for all sites.
The original AIM reproducibility studies included several drug/organism combinations that did not have sufficient number of on-scale MIC results.
Another reproducibility study was conducted and included 10 isolates with on-scale MIC values for the antimicrobials that were not on-scale. Cumulative
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reproducibility data is shown below.
Overall Reproducibility of AIM vs. Autoinoculator I for Gram Positive organisms
| | % Reproducibility (AIM vs. Autoinoculator I) | | |
| --- | --- | --- | --- |
| | Best Case (assuming off scale result is within one well from the mode) | On scale (on scale values only) | Worst case* (assuming off scale result is greater than one well from the mode) |
| AutoReader | 99.8 | 99.9 | 86.4 |
| VIZION | 99.7 | 99.7 | 85.8 |
* Off-scale isolates were used due to unavailability or insufficient number of isolates with on-scale MIC values for some drug/organism combinations
Overall Reproducibility of AIM vs. Autoinoculator I for Streptococcus spp.
| | % Reproducibility (AIM vs. Autoinoculator I) | | |
| --- | --- | --- | --- |
| | Best Case (assuming off scale result is within one well from the mode) | On scale (on scale values only) | Worst case* (assuming off scale result is greater than one well from the mode) |
| AutoReader | 99.8 | 99.7 | 81.2 |
| VIZION | 99.6 | 99.6 | 80.2 |
* Off-scale isolates were used due to unavailability or insufficient number of isolates with on-scale MIC values for some drug/organism combinations
Overall Reproducibility of AIM vs. Autoinoculator I for Haemophilus influenzae.
| | % Reproducibility (AIM vs. Autoinoculator I) | | |
| --- | --- | --- | --- |
| | Best Case (assuming off scale result is within one well from the mode) | On scale (on scale values only) | Worst case* (assuming off scale result is greater than one well from the mode) |
| VIZION | 99.7 | 99.8 | 99.4 |
* Off-scale isolates were used due to unavailability or insufficient number of isolates with on-scale MIC values for some drug/organism combinations
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Overall Reproducibility of AIM vs. Autoinoculator I for C. albicans
| | % Reproducibility (AIM vs. Autoinoculator I) | | |
| --- | --- | --- | --- |
| | Best Case (assuming off scale result is within one well from the mode) | On scale (on scale values only) | Worst case* (assuming off scale result is greater than one well from the mode) |
| Manual Mirror | 99.7 | 99.8 | 99.4 |
* Off-scale isolates were used due to unavailability or insufficient number of isolates with on-scale MIC values for some drug/organism combinations
Even though the MIC values were off-scale for a large number of isolates (varied by drug-organism combinations), which has resulted in low performance based on "worst-case" calculation, the overall reproducibility was considered acceptable, since best-case and on-scale reproducibility were greater than 95%.
b. Linearity/assay reportable range:
Not applicable
c. Traceability, Stability, Expected values (controls, calibrators, or methods):
The FDA and CLSI recommended QC isolates were tested on every test occasion at each clinical site. The QC results obtained using Autoinoculator I and AIM were in range for every day tested.
Quality Control was performed at all sites during the studies using the existing Autoinoculator I and the new Autoinoculator, AIM. Results were read either on a manual mirror, the AutoReader, or the VIZION as appropriate for the organism.
S. aureus ATCC 29213
E. faecalis ATCC 29212, ATCC 51299
S. pneumoniae ATCC 49619
H. influenzae ATCC 49247, ATCC 49766
C. parapsilosis ATCC 22019
C. krusei ATCC 6258
S. aureus ATCC BAA-976 (Cefoxitin screen & Dtest),
S. aureus ATCC BAA-977 (Dtest)
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The QC MIC values obtained by the AIM/Autoinoculator I were comparable. For some drugs, the concentration range was not sufficiently broad to provide definite MIC value for both QC organisms. However, the concentration range was sufficient to evaluate at least one QC organism per drug.
Percentage of results within the acceptable QC range
| | | AutoReader | | VIZION | |
| --- | --- | --- | --- | --- | --- |
| QC Organism(s) | Antimicrobial Agent | Autoinoculator I | AIM | Autoinoculator I | AIM |
| S. aureus ATCC 29213
E. faecalis ATCC 29212 | Chloramphenicol
Ciprofloxacin
Clindamycin
Daptomycin
Erythromycin
Gentamicin
Linezolid
Oxacillin
Penicillin
Quinapristin/Dalfapristin
Rifampin
Tetracycline
Trimethoprim/Sulfamethoxazole
Vancomycin | 100% | 100% | 100% | 100% |
| S. aureus ATCC BAA-977, & ATCC BAA-976 | Inducible Clindamycin (Dtest) | 100% | 100% | 100% | 100% |
| S. aureus ATCC BAA-976, & S. aureus ATCC 29213 | Cefoxitin screen | 100% | 100% | 100% | 100% |
| E. faecalis ATCC 29212, ATCC 51299, & S. aureus ATCC 29213 | Gentamicin 500
Streptomycin 1000 | 100% | 100% | 100% | 100% |
| S. pneumoniae ATCC 49619 | Amoxicillin/Clavulanic Acid
Cefepime
Cefotaxime
Chloramphenicol
Clindamycin | | | | |
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| | | AutoReader | | VIZION | |
| --- | --- | --- | --- | --- | --- |
| QC Organism(s) | Antimicrobial Agent | Autoinoculator I | AIM | Autoinoculator I | AIM |
| | Daptomycin
Erythromycin
Levofloxacin
Linezolid
Meropenem
Penicillin
Trimethoprim/Sulfamethoxazole
Tetracycline
Vancomycin | 100% | 100% | 100% | 100% |
| H. influenzae ATCC 49247 | Amoxicillin/Clavulanic Acid
Ampicillin
Ampicillin/Sulbactam
Cefepime
Cefixime
Ceftriaxone
Chloramphenicol
Clarithromycin
Tetracycline
Trimethoprim/Sulfamethoxazole | 100% | 100% | 100% | 100% |
| H. influenzae ATCC 49766 | Cefaclor
Cefuroxime
Imipenem
Meropenem | 100% | 100% | 100% | 100% |
| C. parapsilosis ATCC 22019
C. krusei ATCC 6258 | 5-Flucytosine
Fluconazole
Itraconazole
Voriconazole | 100% | 100% | 100% | 100% |
MIC results were in range for each drug for at least one Quality Control organism tested. Quality Control results for the Sensititre Susceptibility System using AIM as the inoculator or the existing Autoinoculator I demonstrated that the system could produce the expected quality control results whether results are read on the AutoReader or on the VIZION.
The Sensititre Nephelometer was used at each site to standardize the inoculum and it was calibrated every time it was switched on. Colony counts from QC and in-house source was performed using direct inoculum method and the mean result was within the minimum and maximum ranges" All results were within the expected range.
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d. Detection limit:
Not applicable.
e. Analytical specificity:
Not applicable.
f. Assay cut-off:
Not applicable
2. Comparison studies:
a. Method comparison with predicate device:
Performance was established through a clinical study which was conducted at three sites. The studies were designed to evaluate performance of the updated version of the Autoinoculator, AIM to the existing Autoinoculator I using the Sensititre 18-24 hour susceptibility plates. Specially prepared MIC susceptibility panels containing serial dilutions of selected antimicrobial agents representing various classes of antimicrobial agents were inoculated by either the AIM or the Autoinoculator I. Duplicate plates were inoculated. One was inoculated using the Autoinoculator I and the other using the AIM. Plates were read after 18-24 hours of incubation at 35°C. The plate readings were made either on a manual mirror, the AutoReader, or the VIZION as appropriate for the organism. The MIC results obtained for plates inoculated with Autoinoculator I were compared to those obtained for plates inoculated with the AIM. The criteria outlined in the AST Special Controls Guidance Document were used in evaluation of performance of AIM as follows:
AutoReader results comparing AIM versus Autoinoculator I
VIZION results comparing AIM versus Autoinoculator I
Mirror read results comparing AIM versus Autoinoculator I
Clinical testing was performed on Gram positive isolates (89 S. aureus, 61 Staphylococcus spp., 56 Enterococcus spp., 157 beta hemolytic Streptococcus spp, 84 Streptococcus pneumoniae, and 72 viridans streptococci), 195 isolates of H. influenzae and 303 Candida spp. The growth rate for the clinical and challenge isolates was 100%. The performance evaluations are shown in the tables below.
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# Summary Table (AutoReader)
Clinical and challenge isolate results summary for the AIM vs. Existing Autoinoculator (AutoReader)
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Oxacillin + 2% NaCl | Coagulase Negative Staph | 42 | 19 | 61 | 30 | 98.4 | 96.7 | 100 | 23 | 0 | 38 | 0 | 0 | 0 |
| Oxacillin + 2% NaCl | Staphylococcus aureus | 62 | 27 | 89 | 55 | 100 | 100 | 100 | 47 | 0 | 42 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Penicillin | Coagulase Negative Staph | 42 | 19 | 61 | 39 | 100 | 100 | 100 | 12 | 0 | 12 | 0 | 0 | 0 |
| Penicillin | Enterococcus sp. | 40 | 16 | 56 | 41 | 100 | 100 | 100 | 41 | 0 | 41 | 0 | 0 | 0 |
| Penicillin | Staphylococcus aureus | 62 | 27 | 89 | 30 | 100 | 100 | 100 | 12 | 0 | 12 | 0 | 0 | 0 |
| Penicillin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 5 | 0 | 0 | 0 |
| Penicillin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 6 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Linezolid | Coagulase Negative Staph | 42 | 19 | 61 | 34 | 100 | 100 | 100 | 60 | 0 | 1 | 0 | 0 | 0 |
| Linezolid | Enterococcus sp. | 40 | 16 | 56 | 48 | 100 | 100 | 100 | 51 | 0 | 5 | 0 | 0 | 0 |
| Linezolid | Staphylococcus aureus | 62 | 27 | 89 | 88 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pyogenes | 0 | 6 | 6 | 6 | 100 | 100 | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Rifampin | Coagulase Negative Staph | 42 | 19 | 61 | 1 | 100 | 100 | 100 | 59 | 0 | 2 | 0 | 0 | 0 |
| Rifampin | Enterococcus sp. | 40 | 16 | 56 | 29 | 100 | 100 | 85.7 | 23 | 17 | 16 | 0 | 0 | 8 |
| Rifampin | Staphylococcus aureus | 62 | 27 | 89 | 1 | 100 | 100 | 100 | 87 | 0 | 2 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Chloramphenicol | Coagulase Negative Staph | 42 | 19 | 61 | 57 | 98.4 | 100 | 100 | 58 | 0 | 3 | 0 | 0 | 0 |
| Chloramphenicol | Enterococcus sp. | 40 | 16 | 56 | 46 | 100 | 100 | 94.6 | 43 | 4 | 9 | 0 | 0 | 3 |
| Chloramphenicol | Staphylococcus aureus | 62 | 27 | 89 | 84 | 100 | 100 | 94.4 | 69 | 15 | 5 | 0 | 0 | 5 |
| Chloramphenicol | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus pyogenes | 0 | 6 | 6 | 6 | 100 | 100 | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Clindamycin | Coagulase Negative Staph | 42 | 19 | 61 | 7 | 100 | 100 | 100 | 37 | 2 | 22 | 0 | 0 | 0 |
| Clindamycin | Staphylococcus aureus | 62 | 27 | 89 | 3 | 100 | 100 | 100 | 72 | 0 | 17 | 0 | 0 | 0 |
| Clindamycin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
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| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Clindamycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Tetracycline | Coagulase Negative Staph | 42 | 19 | 61 | 43 | 98.4 | 97.7 | 100 | 43 | 0 | 18 | 0 | 0 | 0 |
| Tetracycline | Enterococcus sp. | 40 | 16 | 56 | 20 | 100 | 100 | 100 | 10 | 0 | 46 | 0 | 0 | 0 |
| Tetracycline | Staphylococcus aureus | 62 | 27 | 89 | 78 | 100 | 100 | 100 | 77 | 0 | 12 | 0 | 0 | 0 |
| Tetracycline | Streptococcus agalactiae | 0 | 5 | 5 | 4 | 100 | 100 | 100 | 1 | 0 | 4 | 0 | 0 | 0 |
| Tetracycline | Streptococcus pyogenes | 0 | 6 | 6 | 5 | 100 | 100 | 100 | 5 | 0 | 1 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Erythromycin | Coagulase Negative Staph | 42 | 19 | 61 | 7 | 98.4 | 85.7 | 98.4 | 24 | 1 | 36 | 0 | 0 | 1 |
| Erythromycin | Enterococcus sp. | 40 | 16 | 56 | 18 | 100 | 100 | 100 | 9 | 13 | 34 | 0 | 0 | 0 |
| Erythromycin | Staphylococcus aureus | 62 | 27 | 89 | 31 | 98.9 | 96.8 | 97.8 | 25 | 6 | 58 | 0 | 0 | 2 |
| Erythromycin | Streptococcus agalactiae | 0 | 5 | 5 | 1 | 100 | 100 | 100 | 4 | 0 | 1 | 0 | 0 | 0 |
| Erythromycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Ciprofloxacin | Coagulase Negative Staph | 42 | 19 | 61 | 32 | 100 | 100 | 100 | 31 | 0 | 30 | 0 | 0 | 0 |
| Ciprofloxacin | Staphylococcus aureus | 62 | 27 | 89 | 61 | 100 | 100 | 100 | 55 | 4 | 30 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Quinapristin/Dalfapristin | Coagulase Negative Staph | 42 | 19 | 61 | 0 | 100 | N/A | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Enterococcus sp. | 40 | 16 | 56 | 32 | 100 | 100 | 100 | 17 | 3 | 36 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Staphylococcus aureus | 62 | 27 | 89 | 0 | 100 | N/A | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Daptomycin | Coagulase Negative Staph | 42 | 19 | 61 | 56 | 100 | 100 | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Enterococcus sp. | 40 | 16 | 56 | 52 | 100 | 100 | 100 | 54 | 0 | 2 | 0 | 0 | 0 |
| Daptomycin | Staphylococcus aureus | 62 | 27 | 89 | 86 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Vancomycin | Coagulase Negative Staph | 42 | 19 | 61 | 54 | 100 | 100 | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Enterococcus sp. | 40 | 16 | 56 | 27 | 100 | 100 | 100 | 28 | 3 | 25 | 0 | 0 | 0 |
| Vancomycin | Staphylococcus aureus | 62 | 27 | 89 | 83 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
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| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Vancomycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Trimethoprim/Sulfamethoxazole | Coagulase Negative Staph | 42 | 19 | 61 | 2 | 100 | 100 | 100 | 36 | 0 | 25 | 0 | 0 | 0 |
| Trimethoprim/Sulfamethoxazole | Staphylococcus aureus | 62 | 27 | 89 | 2 | 100 | 100 | 100 | 87 | 0 | 2 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Gentamicin | Coagulase Negative Staph | 42 | 19 | 61 | 23 | 98.4 | 95.7 | 95.1 | 43 | 3 | 15 | 0 | 0 | 3 |
| Gentamicin | Staphylococcus aureus | 62 | 27 | 89 | 80 | 98.9 | 98.8 | 100 | 85 | 0 | 4 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Streptomycin-1000 ug/mL | Enterococcus sp. | 40 | 16 | 56 | 0 | 100 | N/A | 100 | 36 | 0 | 20 | 0 | 0 | 0 |
| Clindamycin | Streptococcus pneumoniae | 60 | 24 | 84 | 48 | 98.8 | 97.9 | 98.8 | 48 | 0 | 36 | 0 | 0 | 1 |
| Penicillin | Beta hemolytic strep | 27 | 0 | 27 | 7 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Penicillin | Strep viridans | 46 | 25 | 71 | 49 | 100 | 100 | 97.2 | 46 | 17 | 8 | 0 | 0 | 2 |
| Penicillin | Streptococcus agalactiae | 52 | 11 | 63 | 50 | 98.4 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Penicillin | Streptococcus pneumoniae | 60 | 24 | 84 | 68 | 98.8 | 98.5 | 98.8 | 11 | 22 | 51 | 0 | 0 | 1 |
| Penicillin | Streptococcus pyogenes | 53 | 14 | 67 | 0 | 100 | N/A | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Amoxicillin/Clavulanate | Streptococcus pneumoniae | 60 | 24 | 84 | 69 | 98.8 | 98.6 | 95.2 | 64 | 11 | 9 | 0 | 0 | 4 |
| Linezolid | Beta hemolytic strep | 26 | 0 | 26 | 26 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus sp. | 47 | 25 | 72 | 72 | 100 | 100 | 100 | 72 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Chloramphenicol | Beta hemolytic strep | 26 | 0 | 26 | 26 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 98.4 | 63 | 1 | 0 | 0 | 0 | 1 |
| Chloramphenicol | Streptococcus pneumoniae | 60 | 24 | 84 | 55 | 100 | 100 | 100 | 55 | 0 | 29 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus sp. | 47 | 25 | 72 | 67 | 100 | 100 | 100 | 72 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Cefepime | Beta hemolytic strep | 27 | 0 | 27 | 27 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Cefepime | Streptococcus agalactiae | 52 | 11 | 63 | 62 | 100 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Cefepime | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 98.8 | 98.8 | 92.9 | 54 | 27 | 3 | 0 | 0 | 6 |
{13}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Cefepime | Streptococcus pyogenes | 53 | 14 | 67 | 26 | 98.5 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Cefotaxime | Beta hemolytic strep | 27 | 0 | 27 | 18 | 96.3 | 94.4 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Cefotaxime | Strep viridans | 46 | 25 | 71 | 62 | 98.6 | 98.4 | 97.2 | 63 | 4 | 4 | 0 | 0 | 2 |
| Cefotaxime | Streptococcus agalactiae | 52 | 11 | 63 | 61 | 100 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Cefotaxime | Streptococcus pneumoniae | 60 | 24 | 84 | 73 | 100 | 100 | 97.6 | 64 | 14 | 6 | 0 | 0 | 2 |
| Cefotaxime | Streptococcus pyogenes | 53 | 14 | 67 | 2 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Tetracycline | Beta hemolytic strep | 27 | 0 | 27 | 18 | 100 | 100 | 100 | 15 | 3 | 9 | 0 | 0 | 0 |
| Tetracycline | Streptococcus agalactiae | 52 | 11 | 63 | 10 | 100 | 100 | 100 | 10 | 0 | 53 | 0 | 0 | 0 |
| Tetracycline | Streptococcus pneumoniae | 60 | 24 | 84 | 35 | 100 | 100 | 98.8 | 35 | 0 | 49 | 0 | 0 | 1 |
| Tetracycline | Streptococcus pyogenes | 53 | 14 | 67 | 57 | 98.5 | 98.2 | 100 | 56 | 1 | 10 | 0 | 0 | 0 |
| Tetracycline | Streptococcus sp. | 47 | 25 | 72 | 51 | 100 | 100 | 97.2 | 49 | 2 | 21 | 0 | 0 | 2 |
| | | | | | | | | | | | | | | |
| Erythromycin | Beta hemolytic strep | 26 | 0 | 26 | 15 | 100 | 100 | 100 | 16 | 0 | 10 | 0 | 0 | 0 |
| Erythromycin | Streptococcus agalactiae | 53 | 11 | 64 | 38 | 100 | 100 | 100 | 38 | 0 | 26 | 0 | 0 | 0 |
| Erythromycin | Streptococcus pneumoniae | 60 | 24 | 84 | 40 | 100 | 100 | 98.8 | 39 | 1 | 44 | 0 | 0 | 1 |
| Erythromycin | Streptococcus pyogenes | 53 | 14 | 67 | 58 | 100 | 100 | 100 | 58 | 0 | 9 | 0 | 0 | 0 |
| Erythromycin | Streptococcus sp. | 47 | 25 | 72 | 33 | 100 | 100 | 100 | 29 | 0 | 43 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Levofloxacin | Beta hemolytic strep | 26 | 0 | 26 | 24 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus pneumoniae | 60 | 24 | 84 | 83 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus pyogenes | 53 | 14 | 67 | 66 | 100 | 100 | 100 | 66 | 1 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus sp. | 47 | 25 | 72 | 69 | 100 | 100 | 100 | 68 | 0 | 4 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Meropenem | Beta hemolytic strep | 26 | 0 | 26 | 6 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus agalactiae | 53 | 11 | 64 | 49 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus pneumoniae | 60 | 24 | 84 | 64 | 100 | 100 | 97.6 | 35 | 26 | 23 | 0 | 0 | 2 |
| Meropenem | Streptococcus pyogenes | 53 | 14 | 67 | 0 | 100 | N/A | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus sp. | 47 | 25 | 72 | 34 | 100 | 100 | 100 | 65 | 0 | 7 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
{14}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Daptomycin | Beta hemolytic strep | 27 | 0 | 27 | 27 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus agalactiae | 53 | 11 | 64 | 63 | 100 | 100 | 98.4 | 64 | 0 | 0 | 0 | 1 | 0 |
| Daptomycin | Streptococcus pyogenes | 53 | 14 | 67 | 64 | 98.5 | 98.4 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus sp. | 47 | 25 | 72 | 64 | 100 | 100 | 100 | 64 | 0 | 8 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Vancomycin | Beta hemolytic strep | 26 | 0 | 26 | 26 | 96.2 | 96.2 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus sp. | 47 | 25 | 72 | 71 | 100 | 100 | 100 | 71 | 0 | 1 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Trimethoprim/Sulfamethoxazole | Streptococcus pneumoniae | 60 | 24 | 84 | 35 | 100 | 100 | 96.4 | 20 | 17 | 47 | 0 | 0 | 3 |
{15}
Clinical and challenge isolate results summary for the AIM vs. Existing Autoinoculator (VIZION)
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Oxacillin + 2% NaCl | Coagulase Negative Staph | 42 | 19 | 61 | 30 | 98.4 | 96.7 | 100 | 23 | 0 | 38 | 0 | 0 | 0 |
| Oxacillin + 2% NaCl | Staphylococcus aureus | 62 | 27 | 89 | 55 | 100 | 100 | 100 | 47 | 0 | 42 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Penicillin | Coagulase Negative Staph | 42 | 19 | 61 | 39 | 100 | 100 | 100 | 12 | 0 | 12 | 0 | 0 | 0 |
| Penicillin | Enterococcus sp. | 40 | 16 | 56 | 41 | 100 | 100 | 100 | 41 | 0 | 41 | 0 | 0 | 0 |
| Penicillin | Staphylococcus aureus | 62 | 27 | 89 | 30 | 100 | 100 | 100 | 12 | 0 | 12 | 0 | 0 | 0 |
| Penicillin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 5 | 0 | 0 | 0 |
| Penicillin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 6 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Linezolid | Coagulase Negative Staph | 42 | 19 | 61 | 34 | 100 | 100 | 100 | 60 | 0 | 1 | 0 | 0 | 0 |
| Linezolid | Enterococcus sp. | 40 | 16 | 56 | 48 | 100 | 100 | 100 | 51 | 0 | 5 | 0 | 0 | 0 |
| Linezolid | Staphylococcus aureus | 62 | 27 | 89 | 88 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pyogenes | 0 | 6 | 6 | 6 | 100 | 100 | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Rifampin | Coagulase Negative Staph | 42 | 19 | 61 | 1 | 100 | 100 | 100 | 59 | 0 | 2 | 0 | 0 | 0 |
| Rifampin | Enterococcus sp. | 40 | 16 | 56 | 29 | 100 | 100 | 85.7 | 23 | 17 | 16 | 0 | 0 | 8 |
| Rifampin | Staphylococcus aureus | 62 | 27 | 89 | 1 | 100 | 100 | 100 | 87 | 0 | 2 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Chloramphenicol | Coagulase Negative Staph | 42 | 19 | 61 | 57 | 98.4 | 100 | 100 | 58 | 0 | 3 | 0 | 0 | 0 |
| Chloramphenicol | Enterococcus sp. | 40 | 16 | 56 | 46 | 100 | 100 | 94.6 | 43 | 4 | 9 | 0 | 0 | 3 |
| Chloramphenicol | Staphylococcus aureus | 62 | 27 | 89 | 84 | 100 | 100 | 94.4 | 69 | 15 | 5 | 0 | 0 | 5 |
| Chloramphenicol | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus pyogenes | 0 | 6 | 6 | 6 | 100 | 100 | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Clindamycin | Coagulase Negative Staph | 42 | 19 | 61 | 7 | 100 | 100 | 100 | 37 | 2 | 22 | 0 | 0 | 0 |
| Clindamycin | Staphylococcus aureus | 62 | 27 | 89 | 3 | 100 | 100 | 100 | 72 | 0 | 17 | 0 | 0 | 0 |
| Clindamycin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Clindamycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Tetracycline | Coagulase Negative Staph | 42 | 19 | 61 | 43 | 98.4 | 97.7 | 100 | 43 | 0 | 18 | 0 | 0 | 0 |
{16}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Tetracycline | Enterococcus sp. | 40 | 16 | 56 | 20 | 100 | 100 | 100 | 10 | 0 | 46 | 0 | 0 | 0 |
| Tetracycline | Staphylococcus aureus | 62 | 27 | 89 | 78 | 100 | 100 | 100 | 77 | 0 | 12 | 0 | 0 | 0 |
| Tetracycline | Streptococcus agalactiae | 0 | 5 | 5 | 4 | 100 | 100 | 100 | 1 | 0 | 4 | 0 | 0 | 0 |
| Tetracycline | Streptococcus pyogenes | 0 | 6 | 6 | 5 | 100 | 100 | 100 | 5 | 0 | 1 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Erythromycin | Coagulase Negative Staph | 42 | 19 | 61 | 7 | 98.4 | 85.7 | 98.4 | 24 | 1 | 36 | 0 | 0 | 1 |
| Erythromycin | Enterococcus sp. | 40 | 16 | 56 | 18 | 100 | 100 | 100 | 9 | 13 | 34 | 0 | 0 | 0 |
| Erythromycin | Staphylococcus aureus | 62 | 27 | 89 | 31 | 98.9 | 96.8 | 97.8 | 25 | 6 | 58 | 0 | 0 | 2 |
| Erythromycin | Streptococcus agalactiae | 0 | 5 | 5 | 1 | 100 | 100 | 100 | 4 | 0 | 1 | 0 | 0 | 0 |
| Erythromycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Ciprofloxacin | Coagulase Negative Staph | 42 | 19 | 61 | 32 | 100 | 100 | 100 | 31 | 0 | 30 | 0 | 0 | 0 |
| Ciprofloxacin | Staphylococcus aureus | 62 | 27 | 89 | 61 | 100 | 100 | 100 | 55 | 4 | 30 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Quinapristin/Dalfapristin | Coagulase Negative Staph | 42 | 19 | 61 | 0 | 100 | N/A | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Enterococcus sp. | 40 | 16 | 56 | 32 | 100 | 100 | 100 | 17 | 3 | 36 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Staphylococcus aureus | 62 | 27 | 89 | 0 | 100 | N/A | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Quinapristin/Dalfapristin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Daptomycin | Coagulase Negative Staph | 42 | 19 | 61 | 56 | 100 | 100 | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Enterococcus sp. | 40 | 16 | 56 | 52 | 100 | 100 | 100 | 54 | 0 | 2 | 0 | 0 | 0 |
| Daptomycin | Staphylococcus aureus | 62 | 27 | 89 | 86 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus agalactiae | 0 | 5 | 5 | 5 | 100 | 100 | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Vancomycin | Coagulase Negative Staph | 42 | 19 | 61 | 54 | 100 | 100 | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Enterococcus sp. | 40 | 16 | 56 | 27 | 100 | 100 | 100 | 28 | 3 | 25 | 0 | 0 | 0 |
| Vancomycin | Staphylococcus aureus | 62 | 27 | 89 | 83 | 100 | 100 | 100 | 89 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus agalactiae | 0 | 5 | 5 | 0 | 100 | N/A | 100 | 5 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus pyogenes | 0 | 6 | 6 | 0 | 100 | N/A | 100 | 6 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Trimethoprim/Sulfamethoxazole | Coagulase Negative Staph | 42 | 19 | 61 | 2 | 100 | 100 | 100 | 36 | 0 | 25 | 0 | 0 | 0 |
{17}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Trimethoprim/Sulfamethoxazole | Staphylococcus aureus | 62 | 27 | 89 | 2 | 100 | 100 | 100 | 87 | 0 | 2 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Gentamicin | Coagulase Negative Staph | 42 | 19 | 61 | 23 | 98.4 | 95.7 | 95.1 | 43 | 3 | 15 | 0 | 0 | 3 |
| Gentamicin | Staphylococcus aureus | 62 | 27 | 89 | 80 | 98.9 | 98.8 | 100 | 85 | 0 | 4 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Streptomycin-1000 ug/mL | Enterococcus sp. | 40 | 16 | 56 | 0 | 100 | N/A | 100 | 36 | 0 | 20 | 0 | 0 | 0 |
| Clindamycin | Streptococcus pneumoniae | 60 | 24 | 84 | 48 | 98.8 | 97.9 | 98.8 | 48 | 0 | 36 | 0 | 0 | 1 |
| Penicillin | Beta hemolytic strep | 27 | 0 | 27 | 7 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Penicillin | Strep viridans | 46 | 25 | 71 | 49 | 100 | 100 | 97.2 | 46 | 17 | 8 | 0 | 0 | 2 |
| Penicillin | Streptococcus agalactiae | 52 | 11 | 63 | 50 | 98.4 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Penicillin | Streptococcus pneumoniae | 60 | 24 | 84 | 68 | 98.8 | 98.5 | 98.8 | 11 | 22 | 51 | 0 | 0 | 1 |
| Penicillin | Streptococcus pyogenes | 53 | 14 | 67 | 0 | 100 | N/A | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Amoxicillin/Clavulanate | Streptococcus pneumoniae | 60 | 24 | 84 | 69 | 98.8 | 98.6 | 95.2 | 64 | 11 | 9 | 0 | 0 | 4 |
| Linezolid | Beta hemolytic strep | 26 | 0 | 26 | 26 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Linezolid | Streptococcus sp. | 47 | 25 | 72 | 72 | 100 | 100 | 100 | 72 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Chloramphenicol | Beta hemolytic strep | 26 | 0 | 26 | 26 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 98.4 | 63 | 1 | 0 | 0 | 0 | 1 |
| Chloramphenicol | Streptococcus pneumoniae | 60 | 24 | 84 | 55 | 100 | 100 | 100 | 55 | 0 | 29 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Chloramphenicol | Streptococcus sp. | 47 | 25 | 72 | 67 | 100 | 100 | 100 | 72 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Cefepime | Beta hemolytic strep | 27 | 0 | 27 | 27 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Cefepime | Streptococcus agalactiae | 52 | 11 | 63 | 62 | 100 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Cefepime | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 98.8 | 98.8 | 92.9 | 54 | 27 | 3 | 0 | 0 | 6 |
| Cefepime | Streptococcus pyogenes | 53 | 14 | 67 | 26 | 98.5 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Cefotaxime | Beta hemolytic strep | 27 | 0 | 27 | 18 | 96.3 | 94.4 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
{18}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Cefotaxime | Strep viridans | 46 | 25 | 71 | 62 | 98.6 | 98.4 | 97.2 | 63 | 4 | 4 | 0 | 0 | 2 |
| Cefotaxime | Streptococcus agalactiae | 52 | 11 | 63 | 61 | 100 | 100 | 100 | 63 | 0 | 0 | 0 | 0 | 0 |
| Cefotaxime | Streptococcus pneumoniae | 60 | 24 | 84 | 73 | 100 | 100 | 97.6 | 64 | 14 | 6 | 0 | 0 | 2 |
| Cefotaxime | Streptococcus pyogenes | 53 | 14 | 67 | 2 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Tetracycline | Beta hemolytic strep | 27 | 0 | 27 | 18 | 100 | 100 | 100 | 15 | 3 | 9 | 0 | 0 | 0 |
| Tetracycline | Streptococcus agalactiae | 52 | 11 | 63 | 10 | 100 | 100 | 100 | 10 | 0 | 53 | 0 | 0 | 0 |
| Tetracycline | Streptococcus pneumoniae | 60 | 24 | 84 | 35 | 100 | 100 | 98.8 | 35 | 0 | 49 | 0 | 0 | 1 |
| Tetracycline | Streptococcus pyogenes | 53 | 14 | 67 | 57 | 98.5 | 98.2 | 100 | 56 | 1 | 10 | 0 | 0 | 0 |
| Tetracycline | Streptococcus sp. | 47 | 25 | 72 | 51 | 100 | 100 | 97.2 | 49 | 2 | 21 | 0 | 0 | 2 |
| | | | | | | | | | | | | | | |
| Erythromycin | Beta hemolytic strep | 26 | 0 | 26 | 15 | 100 | 100 | 100 | 16 | 0 | 10 | 0 | 0 | 0 |
| Erythromycin | Streptococcus agalactiae | 53 | 11 | 64 | 38 | 100 | 100 | 100 | 38 | 0 | 26 | 0 | 0 | 0 |
| Erythromycin | Streptococcus pneumoniae | 60 | 24 | 84 | 40 | 100 | 100 | 98.8 | 39 | 1 | 44 | 0 | 0 | 1 |
| Erythromycin | Streptococcus pyogenes | 53 | 14 | 67 | 58 | 100 | 100 | 100 | 58 | 0 | 9 | 0 | 0 | 0 |
| Erythromycin | Streptococcus sp. | 47 | 25 | 72 | 33 | 100 | 100 | 100 | 29 | 0 | 43 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Levofloxacin | Beta hemolytic strep | 26 | 0 | 26 | 24 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus pneumoniae | 60 | 24 | 84 | 83 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus pyogenes | 53 | 14 | 67 | 66 | 100 | 100 | 100 | 66 | 1 | 0 | 0 | 0 | 0 |
| Levofloxacin | Streptococcus sp. | 47 | 25 | 72 | 69 | 100 | 100 | 100 | 68 | 0 | 4 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Meropenem | Beta hemolytic strep | 26 | 0 | 26 | 6 | 100 | 100 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus agalactiae | 53 | 11 | 64 | 49 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus pneumoniae | 60 | 24 | 84 | 64 | 100 | 100 | 97.6 | 35 | 26 | 23 | 0 | 0 | 2 |
| Meropenem | Streptococcus pyogenes | 53 | 14 | 67 | 0 | 100 | N/A | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Meropenem | Streptococcus sp. | 47 | 25 | 72 | 34 | 100 | 100 | 100 | 65 | 0 | 7 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Daptomycin | Beta hemolytic strep | 27 | 0 | 27 | 27 | 100 | 100 | 100 | 27 | 0 | 0 | 0 | 0 | 0 |
| Daptomycin | Streptococcus agalactiae | 53 | 11 | 64 | 63 | 100 | 100 | 98.4 | 64 | 0 | 0 | 0 | 1 | 0 |
| Daptomycin | Streptococcus pyogenes | 53 | 14 | 67 | 64 | 98.5 | 98.4 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
{19}
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Daptomycin | Streptococcus sp. | 47 | 25 | 72 | 64 | 100 | 100 | 100 | 64 | 0 | 8 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Vancomycin | Beta hemolytic strep | 26 | 0 | 26 | 26 | 96.2 | 96.2 | 100 | 26 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus agalactiae | 53 | 11 | 64 | 64 | 100 | 100 | 100 | 64 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus pneumoniae | 60 | 24 | 84 | 84 | 100 | 100 | 100 | 84 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus pyogenes | 53 | 14 | 67 | 67 | 100 | 100 | 100 | 67 | 0 | 0 | 0 | 0 | 0 |
| Vancomycin | Streptococcus sp. | 47 | 25 | 72 | 71 | 100 | 100 | 100 | 71 | 0 | 1 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Trimethoprim/Sulfamethoxazole | Streptococcus pneumoniae | 60 | 24 | 84 | 35 | 100 | 100 | 96.4 | 20 | 17 | 47 | 0 | 0 | 3 |
Clinical and challenge isolate results summary for the AIM vs. Existing Autoinoculator (VIZION-Site 3)
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Ampicillin | H. influenzae | 46 | 0 | 46 | 11 | 69.6 | 90.9 | 71.7 | 26 | 0 | 20 | 7 | 5 | 1 |
| Amoxacillin/Clavulanate | | 46 | 0 | 46 | 1 | 100 | 100 | 100 | 46 | 0 | 0 | 0 | 0 | 0 |
| Ampicillin/Sulbactam | | 46 | 0 | 46 | 3 | 100 | 100 | 95.7 | 43 | 0 | 3 | 1 | 1 | 0 |
| Chloramphenicol | | 46 | 0 | 46 | 7 | 97.8 | 100 | 97.8 | 46 | 0 | 0 | 0 | 1 | 0 |
| Cefaclor | | 46 | 0 | 46 | 7 | 100 | 100 | 84.8 | 39 | 5 | 2 | 0 | 2 | 5 |
| Cefepime | | 46 | 0 | 46 | 0 | 97.8 | N/A | 100 | 46 | 0 | 0 | 0 | 0 | 0 |
| Cefexime | | 46 | 0 | 46 | 0 | 97.8 | N/A | 100 | 46 | 0 | 0 | 0 | 0 | 0 |
| Ceftriaxone | | 46 | 0 | 46 | 0 | 89.1 | N/A | 93.5 | 39 | 0 | 7 | 2 | 1 | 0 |
| Cefuroxime (sodium) | | 46 | 0 | 46 | 11 | 89.1 | 100 | 100 | 46 | 0 | 0 | 0 | 0 | 0 |
| Tetracycline | | 46 | 0 | 46 | 32 | 87 | 96.9 | 91.3 | 44 | 0 | 2 | 2 | 0 | 2 |
| Clarithromycin | | 46 | 0 | 46 | 25 | 87 | 80 | 69.6 | 21 | 8 | 17 | 3 | 1 | 10 |
| Imipenem | | 46 | 0 | 46 | 1 | 97.8 | 100 | 97.8 | 45 | 0 | 1 | 1 | 0 | 0 |
| Meropenem | | 46 | 0 | 46 | 1 | 93.5 | 100 | 95.7 | 44 | 0 | 2 | 2 | 0 | 0 |
| Trimethoprim/Sulfamethoxazole | | 46 | 0 | 46 | 9 | 76.1 | 77.8 | 76.1 | 28 | 4 | 14 | 4 | 1 | 6 |
{20}
Clinical and challenge isolate results summary for the AIM vs. Existing Autoinoculator (VIZION-Sites 1, 2 and 4)*
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Ampicillin | H. influenzae | 150 | 49 | 199 | 89 | 100 | 100 | 98.9 | 127 | 9 | 63 | 0 | 0 | 2 |
| Amoxacillin/Clavulanate | | 150 | 49 | 199 | 30 | 99.5 | 100 | 99.5 | 169 | 3 | 27 | 0 | 0 | 1 |
| Ampicillin/Sulbactam | | 150 | 49 | 199 | 31 | 100 | 100 | 99.5 | 169 | 0 | 30 | 0 | 1 | 0 |
| Chloramphenicol | | 150 | 49 | 199 | 46 | 100 | 100 | 99.5 | 188 | 2 | 9 | 0 | 0 | 1 |
| Cefaclor | | 150 | 49 | 199 | 31 | 100 | 100 | 97.5 | 179 | 6 | 14 | 0 | 0 | 5 |
| Cefepime | | 150 | 49 | 199 | 13 | 100 | 100 | 100 | 187 | 0 | 12 | 0 | 0 | 0 |
| Cefexime | | 150 | 49 | 199 | 8 | 100 | 100 | 100 | 188 | 0 | 11 | 0 | 0 | 0 |
| Ceftriaxone | | 150 | 49 | 199 | 7 | 100 | 100 | 100 | 190 | 0 | 9 | 0 | 0 | 0 |
| Cefuroxime (sodium) | | 150 | 49 | 199 | 101 | 100 | 100 | 100 | 188 | 2 | 9 | 0 | 0 | 0 |
| Tetracycline | | 150 | 49 | 199 | 186 | 99.5 | 100 | 100 | 196 | 0 | 3 | 0 | 0 | 0 |
| Clarithromycin | | 150 | 49 | 199 | 185 | 100 | 100 | 96.9 | 124 | 63 | 12 | 0 | 0 | 6 |
| Imipenem | | 150 | 49 | 199 | 30 | 100 | 100 | 100 | 190 | 0 | 9 | 0 | 0 | 0 |
| Meropenem | | 150 | 49 | 199 | 24 | 100 | 100 | 100 | 186 | 0 | 13 | 0 | 0 | 0 |
| Trimethoprim/Sulfamethoxazole | | 150 | 49 | 199 | 104 | 100 | 100 | 99.5 | 137 | 18 | 44 | 0 | 0 | 1 |
* Studies with H. influenzae were conducted at 2 external and one internal site. Forty-six H. influenzae isolates, which were originally tested at one of the external sites (site 3), showed unacceptable major error rates (i.e. 3.6 to 19%) and very major error rates (i.e. 17.5 to 100%) with the use of the VIZION for the following drugs: Ampicillin, Chloramphenicol, Cefaclor, Ceftriaxone, Tetracycline, Clarithromycin, Imipenem, Meropenem, and TMP/SMX. This was attributed to site-specific issues of failure to follow on-site training along with failure to confirm the VIZION readings on a mirror viewer. These 46 isolates were later sent to another external laboratory (site 4) for retesting using the VIZION. Site 4 tested the same 46 clinical isolates as site 3 as per the TL. The results presented in this table (3C) reflect the overall results from sites 1, 2 and 4. Please refer to the limitations section.
The following limitation will be included in labeling: "Major and very major errors have occurred when reading H. influenzae results on the VIZION. When using the AIM to inoculate H. influenzae, results obtained by reading on the VIZION should be confirmed with the mirrored viewer."
{21}
Clinical and challenge isolate results summary for the AIM vs. existing Autoinoculator for Cefoxitin Screen Test and Dtest (AutoReader/VIZION)
| Cefoxitin Screen-S. aureus | Total | # CA | % CA | #R | # VMJ | %VMJ | #S | #MAJ | %MAJ |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| AutoReader | 89 | 86 | 96.6 | 41 | 1 | 2.4 | 48 | 2 | 4.2 |
| VIZION | 88 | 87 | 98.9 | 42 | 0 | 0.0 | 46 | 1 | 2.2 |
| | | | | | | | | | |
| Dtest S. aureus | Total | # CA | % CA | #R | # VMJ | %VMJ | #S | #MAJ | %MAJ |
| AutoReader | 89 | 87 | 97.8 | 42 | 1 | 2.4 | 47 | 1 | 2.1 |
| VIZION | 88 | 87 | 98.9 | 42 | 1 | 2.4 | 46 | 0 | 0.0 |
| | | | | | | | | | |
| Dtest Coagulase Negative Staphylococci | Total | # CA | % CA | #R | # VMJ | %VMJ | #S | #MAJ | %MAJ |
| AutoReader | 61 | 61 | 100.0 | 30 | 0 | 0.0 | 31 | 0 | 0.0 |
| VIZION | 61 | 61 | 100.0 | 30 | 0 | 0.0 | 31 | 0 | 0.0 |
The following limitation will be included in labeling: "One major and one very major error occurred when reading S. aureus results on the AutoReader and the VIZION. When using the AIM to inoculate S. aureus for Dtest, consider alternative inoculation methods if inducible clindamycin resistance is suspected."
22
{22}
Clinical and challenge isolate results summary for the AIM vs. existing Autoinoculator (Mirror Read)
| Drug | Organism Group | Clinical | Challenge | Total | Total Evaluable | %EA Total | % EA of Evaluable | %CA | S | I | R or NS | VMJ | MAJ | Minor |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| 5-Flucytocine | C. albicans | 48 | 13 | 61 | 51 | 100 | 100 | 100 | 61 | 0 | 0 | 0 | 0 | 0 |
| | C. glabrata | 17 | 24 | 41 | 1 | 100 | 100 | 100 | 41 | 0 | 0 | 0 | 0 | 0 |
| | C. krusei | 57 | 7 | 64 | 64 | 100 | 100 | 96.9 | 12 | 52 | 0 | 0 | 0 | 2 |
| | C. lusitinae | 15 | 5 | 20 | 1 | 100 | 100 | 100 | 20 | 0 | 0 | 0 | 0 | 0 |
| | C. parapsilosis | 58 | 10 | 68 | 58 | 100 | 100 | 100 | 66 | 0 | 2 | 0 | 0 | 0 |
| | C. tropicalis | 33 | 16 | 49 | 32 | 100 | 100 | 100 | 39 | 0 | 10 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Itraconazole | C. albicans | 48 | 13 | 61 | 57 | 100 | 100 | 96.7 | 50 | 8 | 3 | 0 | 0 | 2 |
| | | | | | | | | | | | | | | |
| Fluconazole | C. albicans | 48 | 13 | 61 | 59 | 100 | 100 | 100 | 59 | 1 | 1 | 0 | 0 | 0 |
| | C. glabrata | 17 | 24 | 41 | 41 | 100 | 100 | 95.1 | 16 | 15 | 10 | 0 | 0 | 2 |
| | C. krusei | 57 | 7 | 64 | 64 | 100 | 100 | 100 | 3 | 27 | 34 | 0 | 0 | 0 |
| | C. lusitinae | 15 | 5 | 20 | 17 | 100 | 100 | 100 | 20 | 0 | 0 | 0 | 0 | 0 |
| | C. parapsilosis | 58 | 10 | 68 | 67 | 100 | 100 | 100 | 66 | 2 | 0 | 0 | 0 | 0 |
| | C. tropicalis | 33 | 16 | 49 | 47 | 100 | 100 | 100 | 46 | 1 | 2 | 0 | 0 | 0 |
| | | | | | | | | | | | | | | |
| Voriconazole | C. albicans | 48 | 13 | 61 | 12 | 100 | 100 | 100 | 60 | 1 | 0 | 0 | 0 | 0 |
| | C. glabrata | 17 | 24 | 41 | 40 | 97.6 | 100 | 100 | 37 | 2 | 2 | 0 | 0 | 0 |
| | C. krusei | 57 | 7 | 64 | 63 | 100 | 100 | 100 | 63 | 0 | 1 | 0 | 0 | 0 |
| | C. lusitinae | 15 | 5 | 20 | 5 | 100 | 100 | 100 | 20 | 0 | 0 | 0 | 0 | 0 |
| | C. parapsilosis | 58 | 10 | 68 | 55 | 100 | 100 | 100 | 68 | 0 | 0 | 0 | 0 | 0 |
| | C. tropicalis | 33 | 16 | 49 | 45 | 100 | 100 | 98 | 47 | 0 | 2 | 0 | 0 | 1 |
{23}
Essential agreement (EA) is when the Sensititre panels inoculated with the AIM produced MIC results that are within +/- one doubling dilution of the results obtained from the Sensititre panels inoculated with Autoinoculator I. Category agreement (CA) is when the Sensititre panel inoculated with the AIM produced interpretative results (SIR) that agreed exactly with those of the Autoinoculator I.
The percent EA is acceptable when compared to the reference method as described in the FDA guidance document, "Class II Special Controls Guidance Document: Antimicrobial Susceptibility Test (AST) Systems; Guidance for Industry and FDA".
Overall, results for all the drugs evaluated were comparable whether the inoculation method was with the existing Autoinoculator I or with the AIM. As shown in the table below, the EA and CA rates were greater than 90% for each group of organisms for all drugs combined.
| Organism/Group | Number of isolates tested | EA (%) | CA (%) |
| --- | --- | --- | --- |
| | AutoReader | | |
| S. aureus | 89 | 99.8 | 99.4 |
| Staphylococcus spp. (CNS) | 61 | 99.4 | 99.5 |
| Enterococcus spp. | 56 | 100 | 98.2 |
| Beta hemolytic Streptococcus spp.(MHB) | 11 | 100 | 100 |
| S. pneumoniae | 84 | 99.2 | 97.7 |
| Viridans Streptococcus spp. | 72 | 99.8 | 99.1 |
| Beta hemolytic group Streptococcus spp. (LHB) | 157 | 99.7 | 99.8 |
| | VIZION | | |
| S. aureus | 88 | 99.9 | 99.2 |
| Staphylococcus spp. (CNS) | 63 | 99.9 | 99.3 |
| Enterococcus spp. | 57 | 100 | 98.9 |
| Beta hemolytic Streptococcus spp.(MHB) | 12 | 100 | 100 |
| S. pneumoniae | 89 | 99.6 | 97.5 |
| Viridans Streptococcus spp. | 72 | 99.3 | 98.4 |
| Beta hemolytic group Streptococcus spp. (LHB) | 156 | 99.8 | 100 |
| | | | |
| Haemophilus influenzae | 195 | 99.5 | 99.2 |
| | Manual Mirror | | |
| Candida spp | 303 | 99.9% | 99.2% |
*MHB= Mueller-Hinton Broth
*LHB = Lysed Horse Blood added to MHB
b. Matrix comparison:
Not Applicable
{24}
3. Clinical Studies:
a. Clinical Sensitivity:
Not Applicable
b. Clinical specificity:
Not Applicable
c. Other clinical supportive data (when a. and b. are not applicable):
Not Applicable
4. Clinical cut-off:
Not Applicable
5. Expected values/Reference range:
Not applicable.
N. Instrument Name:
Sensititre® AIM™
O. System Descriptions:
1. Modes of Operation:
The Autoinoculator 2/AIM is a bench-top instrument which dispenses bacterial suspension (inoculum) into the Sensititre 96-well plate. The instrument has a display which presents options to the End User graphically. After making a selection of the panel layout/configuration, the user may then select the well dose volume (a multiple of 50 µl) specific to each panel section (note that different panel sections may be dosed differently). Having selected these parameters, the user loads the sample, loads a suitable plate and then starts the dosing cycle.
The Autoinoculator 2/AIM is a stand-alone device and requires no connections to other equipment in normal use. It currently provides no support for sample tracking.
2. Software:
FDA has reviewed applicant’s Hazard Analysis and software development processes for this line of product types:
25
{25}
Yes ☐ X ☐ or No ☐
3. Specimen Identification:
The specimen is identified manually by the user. The AIM instrument provides no support for sample tracking.
4. Specimen Sampling and Handling:
The bacterial suspension (inoculum) is prepared by the user. A Sensititre disposable dosehead is affixed to the glass tube containing the final inoculum density which is placed into the instrument's pump assembly. The AIM instrument then dispenses the inoculum into the Sensititre 96-well plate.
5. Calibration:
The AIM instrument is calibrated by weighing inoculated plates. It is recommended that calibration should be carried out at intervals of no less than 1 year.
6. Quality Control:
The AIM instrument uses a built-in routine allowing the adjustment and calibration of the plate dosing. The QC is performed by measuring the weight of a panel before and after dosing, to establish the weight and thus volume of the dosing droplets.
P. Other Supportive Instrument Performance Characteristics Data Not Covered In The "Performance Characteristics" Section above:
Not applicable. All instrument data is included above in section M.
Q. Proposed Labeling:
The labeling is sufficient and satisfies the requirements of 21 CFR Part 809.10.
R. Conclusion:
The submitted information in this premarket notification is complete and supports a substantial equivalence decision.
26
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Learn the FDA Browser
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.