Wondfo Amphetamine Urine Test: Wondfo Amphetamine Urine Test is an immunochromatographic assay for the qualitative determination of d-amphetamine in human urine at a cutoff concentration of 1000 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use. The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive. Wondfo Secobarbital Urine Test: Wondfo Secobarbital Urine Test is an immunochromatographic assay for the qualitative determination of secobarbital in human urine at a cutoff concentration of 300 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use. The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive. Wondfo Oxazepam Urine Test: Wondfo Oxazepam Urine Test is an immunochromatographic assay for the qualitative determination of oxazepam in human urine at a cutoff concentration of 300 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use. The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.
Device Story
Lateral flow immunochromatographic assay for qualitative detection of Amphetamine, Secobarbital, and Oxazepam in human urine; utilizes monoclonal antibody-dye conjugate against drug, gold chloride, fixed drug-protein conjugate, and anti-mouse IgG polyclonal antibody on membrane. Available in strip or cassette formats. Used by healthcare professionals or patients (OTC) for preliminary drug screening. Results interpreted visually; positive results require confirmatory testing via GC/MS. Assists in clinical decision-making regarding drug use status.
Clinical Evidence
No clinical diagnostic data. Performance established via analytical bench testing and a lay-user study. Lay-user study (n=140 per analyte/format) compared device results to GC/MS across various drug concentrations. Overall agreement with GC/MS ranged from 96.4% to 97.8%. Precision studies performed across multiple lots and operators. Specificity and cross-reactivity evaluated against numerous compounds.
Technological Characteristics
Lateral flow immunochromatographic assay; competitive binding principle. Components include monoclonal antibody-dye conjugate, gold chloride, fixed drug-protein conjugate, and anti-mouse IgG polyclonal antibody. Form factors: strip or cassette. No electronic components, software, or external energy source required.
Indications for Use
Indicated for qualitative detection of d-amphetamine (1000 ng/mL), secobarbital (300 ng/mL), or oxazepam (300 ng/mL) in human urine. Intended for prescription and over-the-counter use as a preliminary screening test.
Regulatory Classification
Identification
An amphetamine test system is a device intended to measure amphetamine, a central nervous system stimulating drug, in plasma and urine. Measurements obtained by this device are used in the diagnosis and treatment of amphetamine use or overdose and in monitoring levels of amphetamine to ensure appropriate therapy.
Special Controls
*Classification.* Class II (special controls). An amphetamine test system is not exempt if it is intended for any use other than employment or insurance testing or is intended for Federal drug testing programs. The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 862.9, provided the test system is intended for employment and insurance testing and includes a statement in the labeling that the device is intended solely for use in employment and insurance testing, and does not include devices intended for Federal drug testing programs (*e.g.,* programs run by the Substance Abuse and Mental Health Services Administration (SAMHSA), the Department of Transportation (DOT), and the U.S. military).
Predicate Devices
Acon Laboratories, Inc. One Step Drug Screen Test Card (K020771)
Submission Summary (Full Text)
{0}
510(k) SUBSTANTIAL EQUIVALENCE DETERMINATION
DECISION SUMMARY
ASSAY ONLY TEMPLATE
A. 510(k) Number:
k111560
B. Purpose for Submission:
New device
C. Measurand:
d-Amphetamine, Secobarbital, Oxazepam
D. Type of Test:
Qualitative lateral flow chromatographic immunoassay
E. Applicant:
Guangzhou Wondfo Biotech Co., Ltd.
F. Proprietary and Established Names:
Wondfo Amphetamine Urine Test
Wondfo Secobarbital Urine Test
Wondfo Oxazepam Urine Test
G. Regulatory Information:
1. Regulation section:
21 CFR §862.3100, Amphetamine Test System
21 CFR §862.3150, Barbiturate Test System
21 CFR §862.3170, Benzodiazepine Test System
2. Classification:
All are Class II
3. Product code:
DKZ, DIS, JXM
{1}
Page 2 of 29
4. Panel:
Toxicology (91)
**H. Intended Use:**
1. Intended use(s):
See indications for use below.
2. Indications(s) for use:
**Wondfo Amphetamine Urine Test:**
Wondfo Amphetamine Urine Test is an immunochromatographic assay for the qualitative determination of d-amphetamine in human urine at a cutoff concentration of 1000 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use.
The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.
**Wondfo Secobarbital Urine Test:**
Wondfo Secobarbital Urine Test is an immunochromatographic assay for the qualitative determination of secobarbital in human urine at a cutoff concentration of 300 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use.
The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.
**Wondfo Oxazepam Urine Test:**
Wondfo Oxazepam Urine Test is an immunochromatographic assay for the qualitative determination of oxazepam in human urine at a cutoff concentration of 300 ng/mL. The test is available in a cassette format and a strip format. It is intended for prescription use and over the counter use.
The test provides only preliminary test results. A more specific alternative chemical method must be used in order to obtain a confirmed analytical result. GC/MS is the
{2}
Page 3 of 29
preferred confirmatory method. Clinical consideration and professional judgment should be exercised with any drug of abuse test result, particularly when the preliminary result is positive.
3. Special conditions for use statement(s):
For prescription and over-the counter use.
4. Special instrument requirements:
Not Applicable
I. Device Description:
The tests are in different formats: strip, cassette.
The strip format is a urine test. It is a rapid test for the qualitative detection of the d-amphetamine, secobarbital, and oxazepam. It is a lateral flow chromatographic immunoassay. When the absorbent end of the test device is immersed into the urine sample, the urine is absorbed into the device by capillary action, mixes with the antibody-dye conjugate, and flows across the pre-coated membrane. When the amphetamine, secobarbital, and oxazepam levels are zero or below the target cut off (the detection sensitivity of the test), antibody-dye conjugate binds to the drug-protein conjugate immobilized in the Test Region (T) of the device. This produces a colored Test line, which regardless of its intensity, indicates a negative result.
When amphetamine, secobarbital, and oxazepam levels are at or above the target cutoff, the free drug in the binding sample binds to the antibody-dye conjugate preventing the antibody-dye conjugate from binding to the drug-protein conjugate immobilized in the Test region (T) of the device. This prevents the development of a distinct colored band in the test region, indicating a potentially positive result.
To serve as a procedure control, a colored line will appear at the Control Region (C), if the test has been performed properly because of the antibody-dye conjugate binding to antimouse IgG immobilized in the Control Region of the device.
The Cassette format comes as a test device for amphetamine, secobarbital, and oxazepam. The cassette format is the same function or performance specification of strip. It is composed of a functional strip and a plastic cover, which is a supporting container.
J. Substantial Equivalence Information:
1. Predicate device name(s):
{3}
Page 4 of 29
ACON One Step Drug Screen Test Card
2. Predicate 510(k) number(s):
k020771
3. Comparison with predicate:
| Reagent Similarities and Differences | | |
| --- | --- | --- |
| Feature | Candidate Device: Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Test, and Wondfo Oxazepam Urine Test (k111560) | Predicate Device: ACON One Step Drug Screen Card (k020771) |
| Intended/Indications for Use | For the qualitative determination of d-Amphetamine, Secobarbital, or Oxazepam in human urine. | Same |
| Methodology | Competitive binding, lateral flow immunochromatographic assays based on the principle of antigen-antibody immunochemistry | Same |
| Type of Test | Immunoassay principles that rely on antigen-antibody interactions to indicate positive or negative result | Same |
| Results | Qualitative | Same |
| Specimen Type | Human Urine | Same |
| Cut Off Value | d-Amphetamine: 1000 ng/ml
Secobarbital: 300 ng/ml
Oxazepam: 300 ng/ml | Same |
| Configurations | Strip, Cassette | Card |
| Intended Use | OTC Use & Prescription Use | Prescription Use |
K. Standard/ Guidance Document Referenced (if applicable):
- In Vitro Diagnostic Devices; Guidance for the Preparation of 510(k) Submission
- Premarket Submission and Labeling Recommendations for Drugs of Abuse Screening Tests, Draft Guidance
4
{4}
Page 5 of 29
L. Test Principle:
Immunochromatograph assay using a lateral flow, one step system for the qualitative detection of d-amphetamine, secobarbital and oxazepam in human urine. Each assay uses a mouse monoclonal antibody -dye conjugate against drug with gold chloride and fixed drug-protein conjugate and anti-mouse IgG polyclonal antibody in membrane.
M. Performance Characteristics (if/when applicable):
1. Analytical performance:
a. Precision/Reproducibility:
The precision study was performed by taking negative urine samples and spiking these with: 2000, 1750, 1500, 1250, 1000, 750, 500, 250 and 0 ng/ml of d-amphetamine, corresponding to ± 25, 50, 75, and 100% of the 1000 ng/ml cut-off value; 600, 525, 450, 375, 300, 225, 150, 750 and 0 ng/ml of secobarbital, corresponding to ± 25, 50, 75, and 100% of the 300 ng/ml cut-off value; and 600, 525, 450, 375, 300, 225, 150, 750 and 0 ng/ml of oxazepam, corresponding to ± 25, 50, 75, and 100% of the 300 ng/ml cut-off value. Two sets of operators performed the testing (group A ran the strip format and group B ran the cassette format) and the samples were divided into 12 sets of 25 (one set per lot per run for each format). Three lots of the strip and three lots of the cassette formats of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Test, and Wondfo Oxazepam Urine Test were used. Each of three operators tested 2 aliquot at each concentration for each lot per day (2 runs per day for 25 days), resulting in a total of 50 determinations by each operator at each concentration. The operators were blinded. A summary of the results is presented in the tables below.
a. Strip Format
d-Amphetamine
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 5/45 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50-0 | 50/0 | 50/0 | 50/0 | 3/47 | 0/50 | 0/50 | 0/50 | 0/50 |
Secobarbital
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
5
{5}
Page 6 of 29
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 5/45 | 0/50 | 0/50 | 0/50 | 0/50 |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
## Oxazepam
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 7/43 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
## b. Cassette Format
### d-Amphetamine
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50/0 | 50/0 | 50/0 | 50/0 | 5/45 | 0/50 | 0/50 | 0/50 | 0/50 |
### Secobarbital
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 7/43 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50/0 | 50/0 | 50/0 | 50/0 | 5/45 | 0/50 | 0/50 | 0/50 | 0/50 |
6
{6}
Page 7 of 29
Oxazepam
| Lot | -100% Cut-off | -75% Cut-off | -50% Cut-off | -25% Cut-off | Cut-off | +25% Cut-off | +50% Cut-off | +75% Cut-off | + 100% Cut-off |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Neg/Pos | Ne/Pos | Neg/Pos | Neg/Pos | Neg/Pos |
| Lot 1 | 50/0 | 50/0 | 50/0 | 50/0 | 7/43 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 2 | 50/0 | 50/0 | 50/0 | 50/0 | 6/44 | 0/50 | 0/50 | 0/50 | 0/50 |
| Lot 3 | 50/0 | 50/0 | 50/0 | 50/0 | 5/45 | 0/50 | 0/50 | 0/50 | 0/50 |
b. Linearity/assay reportable range:
Not Applicable, the assay is intended for qualitative use
c. Traceability, Stability, Expected values (controls, calibrators, or methods):
Control standards are not supplied with this device; however, this device has internal process controls. A colored line appearing in the control region confirms sufficient sample volume and adequate membrane wicking. Users are informed that the test is invalid if a line fails to appear in the control region.
Stability
Accelerated stability and real time stability tests were performed on three batches of strip and cassette Wondfo Amphetamine Urine Tests, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests. Accelerated stability was performed at 50°C for 1 month to support a one year shelf life and for 2-4 months to support a two year shelf life; the data supports an 18 month shelf life. Real time studies were performed by storing three lots of strips and cassettes at 4°C and 30°C. Performance tests were completed at defined intervals and the results support a 23 month shelf life at 4°C for the Wondfo Secobarbital Urine Test and 24 months for the Wondfo Amphetamine and Wondfo Oxazepam Urine Tests; and 24 month shelf life at 30°C for the Wondfo Secobarbital Urine Test and 23 months for the Wondfo Amphetamine and Wondfo Oxazepam Urine Tests. Shipping studies were performed on three lots of each strip and cassette formats for the Wondfo Amphetamine Urine Tests, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests to simulate the coldest (12°C average temp) and hottest (36.8°C average temp) months of the year. These studies showed that the devices can be used for the international transport environment.
d. Detection limit:
Analytical performance of the device around the cutoff is described in Section f. (Assay cut-off) below.
{7}
Page 8 of 29
e. Analytical specificity:
Specificity and cross-reactivity was performed by using three batches of both the strip and cassette formats of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests. The samples were split into two aliquots and one group of operators ran the strip format on one set of aliquots and a separate group of operators ran the cassette format on the other set of aliquots. Thirty drug-free urine samples were tested and all were found to be negative. Cross-reactivity was determined by spiking the target drug, drug metabolites and the same class compounds that may cross-react with the target drugs into drug-free urine at three different concentrations and measuring the samples in triplicate using three batches of strips and three batches of cassettes.
d-Amphetamine
| AMP (Amphetamine) (d-Amphetamine, Cutoff = 1000 ng/ml) | Result (Positive at 1000 ng/ml) | % Cross Reactivity 100% |
| --- | --- | --- |
| 1-Amphetamine | Positive at 50000 ng/ml | 2% |
| dl-Amphetamine | Positive at 3000 ng/mL | 33% |
| (+/-) 3,4-methylenedioxyamphetamine (MDA) | Positive at 5,000 ng/mL | 20% |
| Phentermine | Positive at 3000 ng/mL | 33% |
Secobarbital
| Secobarbital, Cutoff= 300 ng/ml) | Result (Positive at 300 ng/ml) | % Cross Reactivity 100% |
| --- | --- | --- |
| Amobarbital | Positive at 300 ng/mL | 100% |
| Alphenol | Positive at 150 ng/mL | 200% |
| Aprobarbital | Positive at 200 ng/mL | 150% |
| Butabarbital | Positive at 75 ng/mL | 400% |
| Butathal | Positive at 100 ng/mL | 300% |
8
{8}
Page 9 of 29
| Butalbital | Positive at 2,500 ng/mL | 12% |
| --- | --- | --- |
| Cyclopentobarbital | Positive at 600 ng/mL | 50% |
| Pentobarbital | Positive at 300 ng/mL | 100% |
| Phenobarbital | Positive at 150 ng/mL | 200% |
## Oxazepam
| Oxazepam, Cutoff= 300 ng/ml | Result
Positive at 300 ng/ml | % Cross Reactivity
100% |
| --- | --- | --- |
| Alprazolam | Positive at 200 ng/mL | 150% |
| a-hydroxyalprazolam | Positive at 1,500 ng/mL | 20% |
| Bromazepam | Positive at 1,500 ng/mL | 20% |
| Chlordiazepoxide | Positive at 1,500 ng/mL | 20% |
| Clonazepam HCl | Positive at 800 ng/mL | 37.5% |
| Clobazam | Positive at 100 ng/mL | 300% |
| Clonazepam | Positive at 800 ng/mL | 37.5% |
| Clorazepate dipotassium | Positive at 200 ng/mL | 150% |
| Delorazepam | Positive at 1,500 ng/mL | 20% |
| Desalkylflurazepam | Positive at 400 ng/mL | 75% |
| Diazepam | Positive at 200 ng/mL | 150% |
| Estazolam | Positive at 2,500 ng/mL | 12% |
| Fluintrazepam | Positive at 400 ng/mL | 75% |
| D,L-Lorazepam | Positive at 1,500 ng/mL | 20% |
| Midazolam | Positive at 12,500 ng/mL | 2.4% |
| Nitrazepam | Positive at 100 ng/mL | 300% |
9
{9}
Page 10 of 29
| Norchlordiazepoxide | Positive at 200 ng/mL | 150% |
| --- | --- | --- |
| Nordiazepam | Positive at 400 ng/mL | 75% |
| Temazepam | Positive at 100 ng/mL | 300% |
| Trazolam | Positive at 2,500 ng/mL | 12% |
The following unrelated compounds were found not to cross-react when tested spiked (100 µg/mL) into drug-free urine, as well as into urine spiked with ± 25% of the cut-off concentration of d-amphetamine, secobarbital, or oxazepam individually:
10
{10}
Page 11 of 29
d-Amphetamine:
4-Acetamindophenol
Acetophenetidin
N-acetylprocainamide
Acetylsalicyclic Acid
Aminopyrine
Amitryptyline
Amobarbital
Amoxicillin
Ampicillin
Ascorbic Acid
Apomorphine
Aspartame
Atropine
Benzilic Acid
Benzoic Acid
Benzoylecgonine
Bilirubin
Brompheniramine
Caffeine
Cannabidiol
Cannabinol
Chloralhydrate
Chloramphenicol
Chlordiazepoxide
Chlorothiazide
(+/-) Chlorpheniramine
Chlorpromazine
Chlorquine
Cholesterol
Clomipramine
Clonidine
Cocaine hydrochloride
Codeine
Cortisone
(-) Cotinine
Creatinine
Deoxycorticosterone
Dextromethorphan
Diazepam
Diclofenac
Diflunisal
Digoxin
Diphenydramine
Doxylamine
Ecgonine hydrochloride
Ecgonine methylester
(IR,2S(-(-)-Ephedrine
L-Ephedrine
(-) Y Ephedrine
Erythromycin
b- Estradiol
Estrone-3-sulfate
Ethyl-p-aminobenzoate
Fenfluramine
Fenoprofen
Furosemide
Gentisic acid
Hemoglobin
Hydralazine
Hydrochlorthiazide
Hydrocodone
Hydrocortisone
O-Hydroxyhippuric acid
3-Hydroxytyramine
Ibuprofen
Imipramine
(-) Isoproterenol
Isoxsuprine
Ketamine
Ketoprofen
Labetalol
Levorphanol
Loperamide
Maprotiline
Meperidine
Meprobamate
Methadone
Methylphenidate
Morphine-3-D-glucoronide
Nalidixic acid
Naloxone
Naltrexone
Naproxen
Niacinamide
Nifedipine
Norcodein
Norethindrone
D-Norpropoxyphene
Noscapine
D,L-Octopamine
Oxalic Acid
Oxazepam
Oxolinic Acid
Oxycodone
Oxymetazoline
Papaverine
Penicillin-G
Pentazocaine
Pentobarbital
Perphenazine
Phencyclidine
Phenelzine
Phendimetrazine
Phenobarbitol
Phetoin
L-Phenylephrine
b-Phenylethlamine
Phenylpropanolamine
Prednisolone
Prednisone
Procaine
Promazine
Promethazine
D,L-Propranolol
Propiomazine
D-Propoxyphene
Quinidine
Quinine
Ranitidine
Salicylic Acid
Secobarbital
Serotonin
Sulfamethazine
Sulindac
Temazepam
Tetracycline
Tetrahydrocortisone
Tetrahydrozoline
d9-THC-COOH
Thebaine
Thiamine
Thioridazine
D,L-Thyroxine
Tolbutamine
Triamterene
Trifluoperazine
Trimethoprim
Trimipramine
Tryptamine
D,L- Tyrosine
Uric Acid
Verapamil
Zomepirac
11
{11}
Page 12 of 29
# Secobarbital:
| Acetaminophen | L-Ephedrine | Oxycodone |
| --- | --- | --- |
| Acetophenetidin | Erythromycin | Oxymetazoline |
| N-acetylprocainamide | b-Estradiol | Papaverine |
| Acetylsalicyclic Acid | Estrone-3-sulfate | Penicillin-G |
| Aminopyrine | Ethyl-p-aminobenzoate | Pentazocaine |
| Amitryptyline | Fenfluramine | Perphenazine |
| Amoxicillin | Fenoprofen | Phencyclidine |
| Ampicillin | Furosemide | Phenelzine |
| Ascorbic Acid | Gentisic acid | Phendimetrazine |
| Apomorphine | Hemoglobin | Phetoin |
| Aspartame | Hydralazine | L-Phenylephrine |
| Benzilic Acid | Hydrochlorthiazide | b-Phenylethlamine |
| Benzoic Acid | Hydrocodone | Phenylpropanolamine |
| Benzoylecgonine | Hydrocortisone | Prednisolone |
| Bilirubin | O-Hydroxyhippuric acid | Prednisone |
| Brompheniramine | 3-Hydroxytyramine | Procaine |
| Caffeine | Ibuprofen | Promazine |
| Cannabidiol | Imipramine | Promethazine |
| Cannabinol | (-) Isoproterenol | D,L-Propranolol |
| Chloralhydrate | Isoxsuprine | Propiomazine |
| Chloramphenicol | Ketamine | D-Propoxyphene |
| Chlordiazepoxide | Ketoprofen | Quinidine |
| Chlorothiazide | Labetalol | Quinine |
| (+/-) Chlorpheniramine | Levorphanol | Ranitidine |
| Chlorpromazine | Loperamide | Salicylic Acid |
| Chlorquine | Maprotiline | Serotonin |
| Cholesterol | Meperidine | Sulfamethazine |
| Clomipramine | Meprobamate | Sulindac |
| Clonidine | Methadone | Temazepam |
| Cocaine hydrochloride | Methylphenidate | Tetracycline |
| Codeine | Morphine-3-D-glucoronide | Tetrahydrocortisone |
| Cortisone | Nalidixic acid | Tetrahydrozoline |
| (-) Cotinine | Naloxone | Thiamine |
| Creatinine | Naltrexone | Thioridazine |
| Deoxycorticosterone | Naproxen | D,L-Thyroxine |
| Dextromethorphan | Niacinamide | Tolbutamine |
| Diazepam | Nifedipine | Triamterene |
| Diclofenac | Norcodein | Trifluoperazine |
| Diflunisal | Norethindrone | Trimethoprim |
| Digoxin | D-Norpropoxyphene | Trimipramine |
| Diphenydramine | Noscapine | Tryptamine |
| Doxylamine | D,L-Octopamine | D,L-Tyrosine |
| Ecgonine hydrochloride | Oxalic Acid | Uric Acid |
| Ecgonine methylester | Oxazepam | Verapamil |
| (IR,2S(-(-))-Ephedrine | Oxolinic Acid | Zomepirac |
12
{12}
Page 13 of 29
Oxazepam:
4-
Acetamindophenol
Acetophenetidin
N-
acetylprocainamide
Acetylsalicyclic
Acid
Aminopyrine
Amitryptyline
Amorbarbital
Amoxicillin
Ampicillin
l-Ascorbic Acid
Apormorphine
Asppartame
Atropine
Benzilic Acid
Benzoic Acid
Benzoylecgonine
Bilirubin
Caffeine
Cannabidiol
Chloralhydrate
Chloramphenicol
Chlordiazepoxide
Chlorothiazide
(+/-)
Chlorpheniramine
Chlorpromazine
Chlorquine
Cholesterol
Clomipramine
Clonidine
Cocaine
hydrochloride
Cortisone
(-) Cotinine
Creatinine
Dextromethlorphan
Diazepam
Diclorenac
Diflunisal
(-) Y Ephedrine
Fenoprofen
Furosemide
Gentisic acid
Hemoglobin
Hydrocortisone
O-Hydroxyhippuric acid
p-Hydroxy-methamphetamine
3-Hydroxytyramine
Ibuprofen
Imipramine
Iproniazid
(-) Isoproterenol
Isoxsuprine
Ketamine
Ketoprofen
Loperamide
Maprotiline
Meperidine
Meprobamate
Methadone
Methylphenamine
(+) 3,4-
Methylenedioxymethamphetamine
Nalidixic acid
Nalorphine
Naloxone
Naltrexone
Naproxen
Niacinamide
Nifedipine
Norethindrone
D-Norpropoxyphene
Noscapine
Phencyclidine
Phenelzine
Phenobarbitol
Phenteramine
L-Phenylephrine
b-Phenylethlamine
Phenylpropanolamine
Prednisone
D,L-Propranolol
D-Propoxyphene
D-Pseudoephedrine
Quinine
Ranitidine
Salicylic Acid
Secobarbital
Serotonin (5-
hydroxytyramine)
Sertraline
Sulframethazine
Sulindac
Tetrahydrocortisone, 3
Acetate
Tetrahydrocortisone, (b-D
glucuronide)
Tetrahydrozoline
Thiamine
Thioridazine
D,L-Thyroxine
Tolbutamine
Triamterene
Trifluoperazine
Trimethoprim
Triyptamine
D,L-Tryptophan
Tyramine
Uric Acid
Verapamil
Zomepirac
13
{13}
Page 14 of 29
The pH of a drug-free urine pool was adjusted to pH 4, pH 5, pH 6, pH 7, pH 8 or pH 9; the urine was spiked with ± 25% of the cut-off concentration of d-amphetamine, secobarbital, or oxazepam, individually and tested using three batches of strips and three batches of cassettes of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests, respectively. The spiked, pH-adjusted urine was tested in triplicate. Altering the pH of the urine sample did not affect the accuracy of any of the test results.
The specific gravity of a drug-free urine pool was measured by obtaining urine samples with specific gravities of 1.000-1.035 and spiking with ± 25% of the cut-off concentration of d-amphetamine, secobarbital, or oxazepam, individually using three batches of strips and three batches of cassettes of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests, respectively. The spiked urines of different specific gravities were tested in triplicate. The results indicate that there is stable performance of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Tests when urine has a specific gravity between 1.00-1.035.
f. Assay cut-off:
The assay cut off was investigated by using three batches of both the strip and cassette formats of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Test to test 150 urine samples each. These samples came from the Shezhen Drug Addiction Recovery Center (25 Drug urine samples each for amphetamine, barbiturate, and benzodiazepine) and from drug-free urine samples (125 samples) spiked with d-amphetamine, secobarbital, or oxazepam (125 samples for each drug) diluted from the International Drug Standard (Sigma) to concentrations that are plus and minus 25% and 50% of the cutoff concentrations. Drug concentrations were confirmed by GC/MS. Results were read by three laboratory assistants with relevant experience. The cutoff studies were performed by two separate groups of operators (one for the strip format and one for the cassette format). Three operators in each group performed the readings and they were blinded to the sample. Each result was confirmed by at least two assistants.
a. Strip
d-Amphetamine
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 500 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 750 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 1000 | Cut-off | 30 | 4 | 26 | 2 | 28 | 3 | 27 | 9 | 81 |
| 1250 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
{14}
Page 15 of 29
| 1500 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
Secobarbital
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 150 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 225 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 300 | Cut-off | 30 | 2 | 28 | 3 | 27 | 2 | 28 | 7 | 83 |
| 375 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| 450 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
Oxazepam
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 150 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 225 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 300 | Cut-off | 30 | 3 | 27 | 4 | 26 | 4 | 26 | 11 | 79 |
| 375 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| 400 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
b. Cassette:
d- Amphetamine
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 500 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 750 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 1000 | Cut-off | 30 | 2 | 28 | 4 | 26 | 3 | 27 | 9 | 81 |
| 1250 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| 1500 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
15
{15}
Page 16 of 29
Secobarbital
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 150 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 225 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 300 | Cut-off | 30 | 3 | 27 | 4 | 26 | 4 | 26 | 17 | 79 |
| 375 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| 400 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
Oxazepam
| [Drug] (ng/ml) | Cut-off range | n | Batch 1 | | Batch 2 | | Batch 3 | | Total | |
| --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- |
| | | | - | + | - | + | - | + | - | + |
| 150 | -50% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 225 | -25% Cutoff | 30 | 30 | 0 | 30 | 0 | 30 | 0 | 90 | 0 |
| 300 | Cut-off | 30 | 4 | 26 | 3 | 27 | 2 | 28 | 9 | 81 |
| 375 | +25% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
| 400 | +50% Cut-off | 30 | 0 | 30 | 0 | 30 | 0 | 30 | 0 | 90 |
The cut-off values were determined to be:
| Test | Calibrator | Cut-off (ng/ml) |
| --- | --- | --- |
| Amphetamine | D-Amphetamine | 1000 |
| Secobarbital | Secobarbital | 300 |
| Oxazepam | Oxazepam | 300 |
2. Comparison studies:
a. Method comparison with predicate device:
1. Performance of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Test (strip and cassette formats) was established by comparing 80 samples of each analyte against GC/MS. These samples came from drug-free urine (10 samples each), the Shezhen Drug Addiction Recovery Center (45 samples for each analyte) and from clinical
16
{16}
Page 17 of 29
samples with concentrations ranges as follows: drug free urine, < -50% of the cut-off, -50% of the cut-off to the cut-off, cut-off to +50% of the cut-off, and > +50% of the Cut-off. There were two groups of operators (one for the strip format and one for the cassette format) and they were blinded to the samples. Each result was read by three laboratory assistants with relevant experience and a lay person with no experience other than reading the instructions for use.
a. Strip
d-Amphetamine:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 2 | 11 | 29 |
| | - | 10 | 18 | 10 | 0 | 0 |
| Viewer B | + | 0 | 0 | 2 | 11 | 29 |
| | - | 10 | 18 | 10 | 0 | 0 |
| Viewer C | + | 0 | 0 | 2 | 11 | 29 |
| | - | 10 | 18 | 10 | 0 | 0 |
| Lay Person | + | 0 | 0 | 3 | 11 | 29 |
| | - | 10 | 18 | 9 | 0 | 0 |
Secobarbital:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
| Viewer B | + | 0 | 0 | 1 | 20 | 20 |
| | - | 10 | 10 | 19 | 0 | 0 |
| Viewer C | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
| Lay Person | + | 0 | 0 | 3 | 20 | 20 |
| | - | 10 | 10 | 17 | 0 | 0 |
{17}
Page 18 of 29
Oxazepam:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
| Viewer B | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
| Viewer C | + | 0 | 0 | 1 | 20 | 20 |
| | - | 10 | 10 | 19 | 0 | 0 |
| Lay Person | + | 0 | 0 | 3 | 20 | 20 |
| | - | 10 | 10 | 17 | 0 | 0 |
b. Cassette
d-Amphetamine:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 1 | 11 | 29 |
| | - | 10 | 18 | 11 | 0 | 0 |
| Viewer B | + | 0 | 0 | 2 | 11 | 29 |
| | - | 10 | 18 | 10 | 0 | 0 |
| Viewer C | + | 0 | 0 | 2 | 11 | 29 |
| | - | 10 | 18 | 10 | 0 | 0 |
| Lay Person | + | 0 | 0 | 3 | 11 | 29 |
| | - | 10 | 18 | 9 | 0 | 0 |
Secobarbital:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 1 | 20 | 20 |
| | - | 10 | 10 | 19 | 0 | 0 |
| Viewer B | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
18
{18}
Page 19 of 29
| Viewer C | + | 0 | 0 | 1 | 20 | 20 |
| --- | --- | --- | --- | --- | --- | --- |
| | - | 10 | 10 | 19 | 0 | 0 |
| Lay Person | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
Oxazepam:
| Wondfo Device Result | | Drug-free urine | < -50% of the cut-off | -50% of the cut-off to the cut-off | cut-off to +50% of the cut-off | > +50% of the Cut-off |
| --- | --- | --- | --- | --- | --- | --- |
| Viewer A | + | 0 | 0 | 1 | 20 | 20 |
| | - | 10 | 10 | 19 | 0 | 0 |
| Viewer B | + | 0 | 0 | 1 | 20 | 20 |
| | - | 10 | 10 | 19 | 0 | 0 |
| Viewer C | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
| Lay Person | + | 0 | 0 | 2 | 20 | 20 |
| | - | 10 | 10 | 18 | 0 | 0 |
The discordant results are listed in the table below.
a. Strip:
19
{19}
| Viewer | Sample Number | GC/MS result | Viewer Result |
| --- | --- | --- | --- |
| Viewer A | AMPC62 | 921 | positive |
| Viewer A | AMPC65 | 993 | positive |
| Viewer B | AMPC31 | 818 | positive |
| Viewer B | AMPC65 | 993 | positive |
| Viewer C | APMC31 | 818 | positive |
| Viewer C | AMPC62 | 921 | positive |
| Lay person | AMPC31 | 818 | positive |
| Lay person | AMPC35 | 797 | positive |
| Lay person | APMC65 | 993 | positive |
| Viewer A | BARC34 | 243 | positive |
| Viewer A | BAR216 | 280 | positive |
| Viewer B | BARC34 | 243 | positive |
| Viewer C | BARC35 | 237 | positive |
| Viewer C | BAR216 | 280 | positive |
| Lay person | BARC34 | 243 | positive |
| Lay person | BARC35 | 237 | positive |
| Lay person | BAR216 | 280 | positive |
| Viewer A | BZOC34 | 243 | positive |
| Viewer A | BZOC65 | 277 | positive |
| Viewer B | BZOC32 | 226 | positive |
| Viewer B | BZOC65 | 277 | positive |
| Viewer C | BZOC34 | 243 | positive |
| Lay person | BZOC32 | 226 | positive |
| Lay person | BZOC34 | 243 | positive |
| Lay person | BZOC65 | 277 | positive |
{20}
The results indicate that similar positive, negative and overall agreement rates for all three tests using the strip format.
b. Cassette:
| Viewer | Sample Number | GC/MS result | Viewer Result |
| --- | --- | --- | --- |
| Viewer A | AMPC31 | 818 | positive |
| Viewer B | APMC31 | 818 | positive |
| Viewer B | AMPC62 | 921 | positive |
| Viewer C | AMPC35 | 797 | positive |
| Viewer C | APMC65 | 993 | positive |
| Lay person | AMPC31 | 818 | positive |
| Lay person | AMPC35 | 797 | positive |
| Lay person | APMC65 | 993 | positive |
| Viewer A | BARC35 | 237 | positive |
| Viewer B | BARC34 | 243 | positive |
| Viewer B | BAR216 | 280 | positive |
| Viewer C | BAR216 | 280 | positive |
| Lay person | BARC35 | 237 | positive |
| Lay person | BAR216 | 280 | positive |
| Viewer A | BZOC65 | 277 | positive |
| Viewer B | BZOC34 | 243 | positive |
| Viewer C | BZOC32 | 226 | positive |
| Viewer C | BZOC65 | 277 | positive |
| Lay person | BZOC34 | 243 | positive |
| Lay person | BZOC65 | 277 | positive |
The results indicate that similar positive, negative and overall agreement rates for all three tests using the cassette format.
The overall agreement between the Wondfo devices and GC/MS is presented in the table below:
{21}
Page 22 of 29
| % Agreement | AMP (Strip) | AMP (Cassette) | BAR (Strip) | BAR (Cassette) | BZO (Strip) | BZO (Cassette) |
| --- | --- | --- | --- | --- | --- | --- |
| Positive | 100% | 100% | 100% | 100% | 100% | 100% |
| Negative | 95% | 95.8% | 95.8% | 96.7% | 95.8% | 96.7% |
| Overall | 97.5% | 97.9% | 97.9% | 98.4% | 97.9% | 98.4% |
The overall agreement between the lay viewer and experienced viewer is presented in the table below:
| % Agreement | AMP (Strip) | AMP (Cassette) | BAR (Strip) | BAR (Cassette) | BZO (Strip) | BZO (Cassette) |
| --- | --- | --- | --- | --- | --- | --- |
| Positive | 100% | 100% | 100% | 100% | 100% | 100% |
| Negative | 97.4% | 96.6% | 96.6% | 98.2% | 96.6% | 98.2% |
| Overall | 98.7% | 98.3% | 98.3% | 99.1% | 98.3% | 99.1% |
B. A lay-user study was performed to assess the suitability of the device for home use. Six drug-free urine sample pools were spiked to $\pm 25\%$, $\pm 50\%$, $\pm 75\%$ of the cutoff of target drug, additionally a negative urine pool with no drug was tested. These concentrations were confirmed by GC/MS and aliquoted into 40 individual containers per concentration (20 aliquots per concentration for each strip format). The testing was performed at three sites by 140 blinded consumers divided between three sites (140 users for strip, 140 for cassette for each of the Wondfo Amphetamine Urine Test, Wondfo Secobarbital Urine Tests, and Wondfo Oxazepam Urine Test). The lay users were chosen from likely intended users at the Shenzhen Drug Addiction Recovery Center, The First Affiliated Hospital of Jinan University, and the No. 177 Hospital of the People's Liberation Army. Each participant received the package inset, 1 blinded sample, and either a test strip or cassette. The lay persons test result was compared to the GC/MS result to demonstrate accuracy by lay-users. The following are the results of the lay-user study pooled together from all three sites for the strip format:
{22}
Page 23 of 29
d-Amphetamine:
| % of Cutoff | Number of Samples | d-Amphetamine GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 240.1 | 0/20 | 100 |
| -50 % Cutoff | 20 | 523.4 | 0/20 | 100 |
| -25 % Cutoff | 20 | 721.2 | 2/18 | 90.0 |
| +25% Cutoff | 20 | 1320.5 | 18/2 | 90.0 |
| +50 % Cutoff | 20 | 1465.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 1830.2 | 20/0 | 100 |
Secobarbital:
| % of Cutoff | Number of Samples | Secobarbital GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 86.2 | 0/20 | 100 |
| -50 % Cutoff | 20 | 173.5 | 0/20 | 100 |
| -25 % Cutoff | 20 | 203.4 | 3/17 | 85.0 |
| +25% Cutoff | 20 | 401.6 | 18/2 | 90.0 |
| +50 % Cutoff | 20 | 466.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 560.8 | 20/0 | 100 |
23
{23}
Page 24 of 29
Oxazepam:
| % of Cutoff | Number of Samples | Oxazepam GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 70.2 | 0/20 | 100 |
| -50 % Cutoff | 20 | 168.5 | 0/20 | 100 |
| -25 % Cutoff | 20 | 253.4 | 3/17 | 85.0 |
| +25% Cutoff | 20 | 356.8 | 19/1 | 95.0 |
| +50 % Cutoff | 20 | 482.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 501.6 | 20/0 | 100 |
The following are the results of the lay-user study pooled together from all three sites for the cassette format:
d- Amphetamine:
| % of Cutoff | Number of Samples | d-Amphetamine GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 240.1 | 0/20 | 100 |
| -50 % Cutoff | 20 | 523.4 | 0/20 | 100 |
| -25 % Cutoff | 20 | 721.2 | 2/18 | 90.0 |
| +25% Cutoff | 20 | 1320.5 | 19/1 | 950.0 |
| +50 % Cutoff | 20 | 1465.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 1830.2 | 20/0 | 100 |
24
{24}
Page 25 of 29
Secobarbital:
| % of Cutoff | Number of Samples | Secobarbital GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 86.2 | 0/20 | 100 |
| -50 % Cutoff | 20 | 173.5 | 0/20 | 100 |
| -25 % Cutoff | 20 | 203.4 | 2/18 | 90.0 |
| +25% Cutoff | 20 | 401.6 | 18/2 | 90.0 |
| +50 % Cutoff | 20 | 466.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 560.8 | 20/0 | 100 |
Oxazepam:
| % of Cutoff | Number of Samples | Oxazepam GS/MS Concentration (ng/mL) | Lay person results: Pos/Neg | Percentage of Correct Results |
| --- | --- | --- | --- | --- |
| -100% of the Cut-off | 20 | 0 | 0/20 | 100 |
| -75 % Cutoff | 20 | 70.2 | 0/20 | 100 |
| -50 % Cutoff | 20 | 168.5 | 0/20 | 100 |
| -25 % Cutoff | 20 | 253.4 | 2/18 | 90.0 |
| +25% Cutoff | 20 | 356.8 | 19/1 | 95.0 |
| +50 % Cutoff | 20 | 482.5 | 20/0 | 100 |
| +75 % Cutoff | 20 | 501.6 | 20/0 | 100 |
25
{25}
Page 26 of 29
The overall percent agreement between the Lay person and the GC/MS method was:
| % Agreement | AMP (Strip) | AMP (Cassette) | BAR (Strip) | BAR (Cassette) | BZO (Strip) | BZO (Cassette) |
| --- | --- | --- | --- | --- | --- | --- |
| Total | 97.1% | 97.8% | 96.4% | 97.1% | 97.1% | 97.8% |
C. The subject's were to fill out a questionnaire to evaluate labeling access.
i. Strip format
d-Amphetamine:
The participant's ages ranged from 22-65 and there were slightly more males than females. They come from a variety of career and education backgrounds and none had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn't be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. None of the participants responded that the strip test was difficult, 104/140 said the test was very easy and 36/140 said it was easy. 80/140 said the instructions were very clear and 60/140 said they were clear. 108/140 said the interpretation of the results was very clear and 32/140 said they were clear. When asked what they would do if the device failed to show a result, 105/140 said they would repeat the test with a new test device, 5/140 said they would turn to another method, and 30/140 said they would call the manufacturer if the device failed to show a result.
Secobarbital:
The participant's ages ranged from 22-66 and there were slightly more males than females. They come from a variety of career and education backgrounds and only 1 participant had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn't be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. None of the participants responded that the strip test was difficult, 81/140 said the test was very easy and 59/140 said it was easy. 75/140 said the instructions were very clear and 65/140 said they were clear. 108/140 said the interpretation of the results was very clear and 32/140 said they were clear. When asked what they would do if the device failed to show a result, 111/140 said they would repeat the test with a new test device, 7/140 said they would turn to another method, and 22/140 said they would call the manufacturer if the device failed to show a result.
26
{26}
Page 27 of 29
## Oxazepam:
The participant’s ages ranged from 22-65 and there were slightly more males than females. They come from a variety of career and education backgrounds and only 1 participant had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn’t be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. Only 1 of the participants responded that the strip test was difficult, 81/140 said the test was very easy and 58/140 said it was easy. 66/140 said the instructions were very clear and 74/140 said they were clear. 86/140 said the interpretation of the results was very clear and 54/140 said they were clear. When asked what they would do if the device failed to show a result, 107/140 said they would repeat the test with a new test device, 7/140 said they would turn to another method, and 26/140 said they would call the manufacturer if the device failed to show a result.
ii. Cassette format
## d-Amphetamine:
The participant’s ages ranged from 23-64 and there were slightly more males than females. They come from a variety of career and education backgrounds and only 1 subject had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn’t be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. None of the participants responded that the strip test was difficult, 77/140 said the test was very easy and 63/140 said it was easy. 79/140 said the instructions were very clear and 61/140 said they were clear. 92/140 said the interpretation of the results was very clear and 48/140 said they were clear. When asked what they would do if the device failed to show a result, 113/140 said they would repeat the test with a new test device, 6/140 said they would turn to another method, and 21/140 said they would call the manufacturer if the device failed to show a result.
## Secobarbital:
The participant’s ages ranged from 23-64 and there were slightly more males than females. They come from a variety of career and education backgrounds and only 2 participants had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn’t be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. Only 1 of the participants responded that the strip test was difficult, 76/140 said the test was very easy and 63/140 said it was easy. 71/140 said the instructions were very clear and 69/140 said they were clear. 66/140 said the interpretation of the results was very clear and 74/140 said they were clear. When asked what they would do if the device failed to show a result, 108/140
27
{27}
Page 28 of 29
said they would repeat the test with a new test device, 6/140 said they would turn to another method, and 26/140 said they would call the manufacturer if the device failed to show a result.
**Oxazepam:**
The participant’s ages ranged from 23-69 and there were slightly more males than females. They come from a variety of career and education backgrounds and only none of the participants had used a home drug kit before. They all understood the storage and expiration of the device and that the test could not be reused. They all understood that the strip couldn’t be immersed in urine above the marker line and to read the result within 5 minutes and how to interpret the results. None of the participants responded that the strip test was difficult, 71/140 said the test was very easy and 69/140 said it was easy. 77/140 said the instructions were very clear and 63/140 said they were clear. 82/140 said the interpretation of the results was very clear and 58/140 said they were clear. When asked what they would do if the device failed to show a result, 103/140 said they would repeat the test with a new test device, 11/140 said they would turn to another method, and 26/140 said they would call the manufacturer if the device failed to show a result.
Additionally, a Flesh-Kincaid reading analysis revealed that both package inserts had a reading grade level of 7.
b. **Matrix comparison:**
Not applicable.
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
28
{28}
Page 29 of 29
5. Expected values/Reference range
Specific ranges for each analyte/methodology are listed in the package insert.
N. Proposed Labeling:
The labeling is sufficient and it satisfies the requirements of 21 CFR Part 809.10.
O. Conclusion:
The submitted information in this premarket notification is complete and supports a substantial equivalence decision.
29
Predicate graph will load when search results are available.
Embedding visualization will load when search results are available.
PDF viewer will load when search results are available.
Loading panels...
Select an item from Submissions
Click any panel, subpart, regulation, product code, or device to see details here.
Section Matches
Results will appear here.
Product Code Matches
Results will appear here.
Special Control Matches
Results will appear here.
Loading collections...
Loading
My Alerts
You will receive email notifications based on the filters and frequency you set for each alert.
Sort by:
Create Alert
Search Filters
Agent Token
Create a read-only bearer token for Claude, ChatGPT, or other agents that can call HTTP APIs.
Copy this now. It will not be shown again.
Connected apps
Apps you authorized through browser sign-in. Disconnecting revokes their access immediately.
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.