K120801 · Chison Medical Imaging Co., Ltd. · IYN · Jun 14, 2012 · Radiology
Device Facts
Record ID
K120801
Device Name
CHISON DIAGNOSTIC ULTRASOUND SYSTEM
Applicant
Chison Medical Imaging Co., Ltd.
Product Code
IYN · Radiology
Decision Date
Jun 14, 2012
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 892.1550
Device Class
Class 2
Attributes
Pediatric
Indications for Use
The system is a general-purpose ultrasonic imaging instrument intended for use by a qualified physician for the evaluation of Fetal (Obstetrics), Abdomen, Cardiac (Adult, Pediatric), Small Organ (Thyroid, testes and breast etc), Peripheral Vascular, Transvaginal, Musculo-skeletal (Conventional and Superficial), Pediatric, OB/Gyn and Urology.
Device Story
Integrated preprogrammed color Doppler ultrasound system; available as portable (Q6/Q8) or roll-around (iVis60/iVis60 EXPERT/i7) models. Acquires ultrasound echo data to display images in B-Mode (including Tissue Harmonic Imaging), M-Mode, Pulsed (PW) Doppler, Continuous (CW) Doppler, Color Doppler, Power Doppler, and Directional Power Doppler modes. Used by physicians in clinical settings for diagnostic imaging and fluid flow analysis. System processes received echoes to generate on-screen displays of anatomic structures and fluid flow; supports specialized measurements and calculations. Benefits include non-invasive visualization of internal structures and hemodynamics to aid clinical diagnosis.
Clinical Evidence
Bench testing only. No clinical data provided. Safety and effectiveness supported by compliance with NEMA UD 2, NEMA UD 3, IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, and ISO 10993-1 standards.
Technological Characteristics
Diagnostic ultrasound system; portable or roll-around form factors. Modes: B, M, PW, CW, Color, Power, Directional Power Doppler, Tissue Harmonic Imaging. Transducers: Convex, Micro-convex, Linear, Phased arrays. Connectivity: Standard ultrasound interface. Software-controlled. Complies with IEC 60601-1 (electrical safety), IEC 60601-1-2 (EMC), IEC 60601-2-37 (ultrasound safety), and ISO 10993-1 (biocompatibility).
Indications for Use
Indicated for qualified physicians to perform diagnostic ultrasound imaging and fluid flow analysis in fetal, abdominal, cardiac (adult/pediatric), small organ (thyroid, testes, breast), peripheral vascular, transvaginal, musculoskeletal (conventional/superficial), pediatric, OB/Gyn, and urological applications.
Regulatory Classification
Identification
An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
Predicate Devices
GE Voluson E6/E8 /E8 Expert Diagnostic Ultrasound System (K101236)
Submission Summary (Full Text)
{0}------------------------------------------------
K120801
JUN 1 4 2012
Chison Medical Imaging Co., Ltd
iVis & Q Series, i7 Diagnostic Ultrasound Systems
# PREMARKET NOTIFICATION [510(k)] Summary
This Summary of Safety and Effectiveness is prepared in accordance with 21 CFR Part 807.92(c).
- 1. Company Name: Chison Medical Imaging Co., Ltd. No.8, Xiang Nan Road, Shuo Fang, New District, Wuxi, China 214142 Chison Medical Imaging Co., Ltd. No.8, Xiang Nan Road, Shuo Fang, New District, Wuxi, China 214142
- Contact: Ms. Ruoli Mo Tel: +86-510-85311707, 85310593 Fax: +86-510-85310726
U.S. Agent:
Leiker Regulatory & Quality Consulting 7263 Cronin Circle Dublin, CA 94568
- Contact: Bob Leiker Tel: (925) 556-1302 Fax: (866) 718-3819
- 2. Device Name: CHISON Q8/Q6/ Roll (Portable) Diagnostic Ultrasound System CHISON iVis 60 & iVis 60 EXPERT/i7 (roll-around) Diagnostic Ultrasound System
Common/Usual Name: Diagnostic Ultrasound System with Accessories
Classification: Regulatory Class: II Review Category: Tier II
| Classification Name | 21 CFR Section | Product Code |
|------------------------------------------|----------------|--------------|
| Ultrasonic pulsed doppler imaging system | 892.1550 | 90-IYN |
| Ultrasonic pulsed echo imaging system | 892.1560 | 90-IYO |
| Diagnostic ultrasonic transducer | 892.1570 | 90-ITX |
#### 2. Marketed Device:
K101236, GE Voluson E6/E8 /E8 Expert Diagnostic Ultrasound System
#### 3. Device Description:
The CHISON Q6 / Q8 / iVis60 / iVis60 / EXPERT / i7 ultrasound system is an integrated preprogrammed color Doppler ultrasound imaging system, capable of producing high detail resolution intended for clinical diagnostic imaging applications.
TAB 20
510(k) Summary
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The CHISON ultrasound system can be configured either as a portable model (Q6/Q8), or as a roll-around model on wheels (iVis60 / iVis60 EXPERT/i7). These systems are designed with the latest technology, using the same quality procedure as ultrasound systems which have been available in the market for years.
This CHISON ultrasound system is a general purpose, software controlled, diagnostic ultrasound system. Its basic function is to acquire ultrasound echo data and display the image in B-Mode (including Tissue Harmonic Imaging), M-Mode, Pulsed (PW) Doppler Mode, Continuous (CW) Doppler Mode, Color Doppler Mode, Power Doppler Mode, Directional Power Doppler Mode, or a combination of these modes.
The CHISON Q Models and iVis60 Models and i7 Model, have been designed to meet the following product safety standards: NEMA UD 2, NEMA UD 3, IEC 60601-1, IEC 60601-1-2, IEC 60601-2-37, IEC 10993-1.
#### 4. Indications for Use:
The system is a general-purpose ultrasonic imaging instrument intended for use by a qualified physician for the evaluation of Fetal (Obstetrics), Abdomen, Cardiac (Adult, Pediatric), Small Organ (Thyroid, testes and breast etc), Peripheral Vascular, Transvaginal, Musculo-skeletal (Conventional and Superficial), Pediatric, OB/Gyn and Urology.
#### 5. Comparison to Predicate Device:
The CHISON Q Models and iVis60 Models and i7 Model are of comparable type and substantially equivalent to the current, GE Voluson E8 Diagnostic Ultrasound System (K101236). All systems transmit ultrasonic energy into patients, then perform post processing of received echoes to generate on-screen display of anatomic structures and fluid flow within the body, and have the same intended uses and basic operating modes as the predicate device. All systems allow for specialized measurements of structures and flow, and calculations.
#### 6. Conclusion:
The CHISON Q Models and i7 systems are substantially equivalent in safety and effectiveness to the predicate systems. The systems are intended for diagnostic ultrasound imaging and fluid flow analysis. The systems have the same gray-scale and Doppler capabilities. The systems have acoustic output levels below the applicable FDA limits. The systems are designed to applicable electrical and physical safety standards.
#### End of 510{k) Summary.
TAB 20
# 510(k) Summary
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Image /page/2/Picture/0 description: The image shows the text "DEPARTMENT OF HEALTH & HUMAN SERVICES" in a bold, sans-serif font. The text is arranged on a single line and is centrally aligned. The words are capitalized, and the overall appearance is clean and professional.
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of a stylized eagle or bird-like figure with three curved lines representing its wings or body. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular fashion around the bird-like figure.
Food and Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993
Chison Medical Imaging Co., Ltd. % Mr. Bob Leiker US Agent Leiker Regulatory & Ouality Consulting 7263 Cronin Circle DUBLIN CA 94568 .
JUN 1 4 2012
Re: K120801
Trade/Device Name: CHISON iVis 60EXPERT, O 6/08. i7 Diagnostic Ultrasound Systems Regulation Number: 21 CFR 892.1550 · Regulation Name: Ultrasonic pulsed doppler imaging system Regulatory Class: II Product Code: IYN, IYO, and ITX Dated: May 18, 2012 Received: May 22, 2012
Dear Mr. Leiker:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration.
This determination of substantial equivalence applies to the following transducers intended for use with the CHISON iVis 60EXPERT, Q 6/Q8, i7 Diagnostic Ultrasound Systems, as described in your premarket notification:
## Transducer Model Number
D3C60L Convex Array D4C40L Convex Array D5C20L Convex Array D6C12L Micro-convex Array D7C10L Micro-convex Array D6C15L Convex Array D7L30L Linear Array
D7L60L Linear Array D7L40L Linear Array D3P64L Phased Array D6P64L Phased Array V4C40L Convex Array D10L40L Linear Array
{3}------------------------------------------------
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
This letter will allow you to begin marketing your device as described in your premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus permits your device to proceed to market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices/ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803). please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
If you have any questions regarding the content of this letter, please contact Jeffrey Ballyns at (301) 796-6105.
Sincerely Yours.
Richard D. O'Kane for
Janine M. Morris Acting Director Division of Radiological Devices Office of In Vitro Diagnostic Device Evaluation and Safety Center for Devices and Radiological Health
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# Diagnostic Ultrasound Indications For Use
# 1.3 Indications for Use
The device is a general-purpose ultrasonic imaging instrument intended for use by a qualified physician for evaluation of Fetal (Obstetrics),Abdomen, Cardiac(Adult, Pediatric), Small Organ (Thyroid, testes and breast etc), Peripheral Vascular, Transvaginal, Musculoskeletal (Conventional and Superficial), Pediatric, OB/Gyn and Urology.
---
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety 510K
Prescription Use V (Part 21 CFR 801 Subpart D) AND/OR
Over-The-Counter Use (21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Eva ustion (ODE)
Indications For Use
{5}------------------------------------------------
# Diagnostic Ultrasound Indications For Use
#### CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Diagnostic Ultrasound Pulsed Echo System Diagnostic Ultrasound Pulsed Doppler Imaging System
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
| Clinical Application | | | Mode of Operation | | | | | | | |
|----------------------------------------------------|---------------------------------|---|-------------------|-----|-----|-------------------------------|------------------|----------|-------|--|
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other | |
| Ophthalmic | Ophthalmic | | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | N | N | N | | N | N | Note 1 | N | |
| | Abdominal | N | N | N | N | N | N | Note 1 | N | |
| | Intra-operative (Specify) | | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | | |
| | Laparoscopic | | | | | | | | | |
| | Pediatric | N | N | N | N | N | N | Note 1 | N | |
| | Small Organ[1] (Specify) | N | N | N | | N | N | Note 1 | N | |
| | Neonatal Cephalic | | | | | | | | | |
| | Adult Cephalic | | | | | | | | | |
| | Trans-rectal | | | | | | | | | |
| | Trans-vaginal | N | N | N | | N | N | Note 1 | N | |
| | Trans-urethral | | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | | |
| | Musculo-skeletal (Conventional) | N | N | N | | N | N | Note 1 | N | |
| | Musculo-skeletal (Superficial) | N | N | N | | N | N | Note 1 | N | |
| | Intravascular | | | | | | | | | |
| | Other(Urology) | N | N | N | | N | N | Note 1 | N | |
| | Other (Ob/GYN) | N | N | N | | N | N | Note 1 | N | |
| Cardiac | Cardiac Adult | N | N | N | N | N | N | Note 1 | N | |
| | Cardiac Pediatric | N | N | N | N | N | N | Note 1 | N | |
| | Intravascular (Cardiac) | | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | | |
| | Intra-cardiac | | | | | | | | | |
| | Other (Specify) | | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | N | N | N | | N | N | Note 1 | N | |
| | Other (Specify) | | | | | | | | | |
| N = new indication; P = previously cleared by FDA; | | | | | | E = added under this appendix | | | | |
Note 1: B+M, B+PWD. B+Color Doppler. B+Power Doppler PWD, B+Power Doppler+PWD, B+Power Doppler+PWD Other *: 3-D · 4-D, Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
Additional Comments:
| Prescription Use<br>(Part 21 CFR 801 Subpart D) | AND/OR | Over-The-Counter Use<br>(21 CFR 801 Subpart C) |
|-------------------------------------------------|--------|------------------------------------------------|
|-------------------------------------------------|--------|------------------------------------------------|
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
*Concurrence of CDRH, Office of Device Evaluation (ODE)*
*(Division Sign-Off)*
*Division of Radiological Devices*
*Office of In Vitro Diagnostic Device Evaluation and Safety*
| Section 510(k) | K120801 |
|----------------|---------------------|
| | Indications For Use |
Page 2 of 15
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Chison Medical Imaging Co., Ltd. - iVis 60 & Q Series,i7 Diagnostic Ultrasound Systems CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D3C60L Convex Array
| Clinical Application | | | Mode of Operation | | | | | | | |
|---------------------------|----------------------------------------------------|---|-------------------|-----|-----|-------------------------------|------------------|----------|--------|--|
| | | | | | | | | | | |
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* | |
| Ophthalmic | Ophthalmic | | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | N | N | N | | N | N | Note 1 | N | |
| | Abdominal | N | N | N | | N | N | Note 1 | N | |
| | Intra-operative (Specify) | | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | | |
| | Laparoscopic | | | | | | | | | |
| | Pediatric | | | | | | | | | |
| | Small Organ1 (Specify) | | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | | |
| | Adult Cephalic | | | | | | | | | |
| | Trans-rectal | | | | | | | | | |
| | Trans-vaginal | | | | | | | | | |
| | Trans-urethral | | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | | |
| | Intravascular | | | | | | | | | |
| | Other(Urology) | N | N | N | | N | N | Note 1 | N | |
| | Other (Ob/GYN) | N | N | N | | N | N | Note 1 | N | |
| Cardiac | Cardiac Adult | | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | | |
| | Intra-cardiac | | | | | | | | | |
| | Other (Specify) | | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | | |
| | Other (Specify) | | | | | | | | | |
| | N = new indication; R = previously cleared by FDA; | | | | | E = added under this appendix | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Note 1: B+M. B+PWD, B+Color Doppler. B+Power Doppler, B+Color Doppler+PWD, B+Power Doppler+PWD Other*: Tissue Harmonic Imaging. [1] Small Organ: Thyroid, testes and breast etc.
Additional Comments:
Prescription Use ✓
(Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use *_*
(21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K. K120801
Section 1.3 Indications For Use Page 3 of 15
Section 1.3
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Chison Medical Imaging Co., Ltd. - iVis 60 & Q Series.i7 Diagnostic Ultrasound Systems System: CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems Transducer: D4C40L Convex Array
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|---------------------------------|-------------------|---|-----|-----|-------------------------------|------------------|----------|--------|
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | N | N | N | | N | N | Note 1 | N |
| | Abdominal | N | N | N | | N | N | Note 1 | N |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ1 (Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other (Urology) | N | N | N | | N | N | Note 1 | N |
| | Other (Ob/GYN) | N | N | N | | N | N | Note 1 | N |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| | N = new indication; | | | | | | | | |
| | P = previously cleared by FDA; | | | | | E = added under this appendix | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Note 1: B+M, B+PWD, B+Color Doppler, B+Power Doppler, B+Color Doppler+PWD, B+Power Doppler+PWD Other *: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
**Additional Comments:**
| Prescription Use | <span></span> √ | AND/OR | Over-The-Counter Use |
|-----------------------------|-----------------|--------|------------------------|
| (Part 21 CFR 801 Subpart D) | | | (21 CFR 801 Subpart C) |
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
| 510K | K120801 |
|------|---------|
|------|---------|
| Section 1.3 | Indications For Use | Page 4 of 15 |
|-------------|---------------------|--------------|
|-------------|---------------------|--------------|
{8}------------------------------------------------
CHISON iVis 60/ iVis 60EXPERT. Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D5C20L Convex Array
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|---------------------------------|-------------------|---|-----|-----|------------------|------------------|----------|--------|
| | | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | | | | | | | | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal<br>Abdominal | N | N | N | N | N | N | Note 1 | N |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | N | N | N | N | N | N | Note 1 | N |
| | Small Organ[1] (Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other(Urology) | | | | | | | | |
| | Other (Ob/GYN) | | | | | | | | |
| Cardiac | Cardiac Adult | N | N | N | N | N | N | Note 1 | N |
| | Cardiac Pediatric | N | N | N | N | N | N | Note 1 | N |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | |
| | Other (Specify) | | | | | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
P = previously cleared by FDA; N = new indication;
E = added under this appendix
Note 1: B+M, B+PWD, B+Color Doppler, B+Power Doppler, B+Color Doppler+PWD. B+Power Doppler+PWD Other*: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
Additional Comments:
Prescription Use ✓
(Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use *_*_
(21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
Secti510K3 K120801
Indications For Use
Page 5 of 15
{9}------------------------------------------------
CHISON iVis 60/ iVis 60EXPERT. Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D6C12L Micro-convex Array
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|---------------------------------|-------------------|---|-----|-----|------------------|------------------|----------|--------|
| | | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | | | | | | | | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | | | | | | | | |
| | Abdominal | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ[1](Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans- rectal | | | | | | | | |
| | Trans- vaginal | N | N | N | | N | N | Note 1 | N |
| | Trans- urethral | | | | | | | | |
| | Trans- esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other(Urology) | N | N | N | | N | N | Note 1 | N |
| | Other (Ob/GYN) | N | N | N | | N | N | Note 1 | N |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | |
| | Other (Specify) | | | | | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
N = new indication; P = previously cleared by FDA; E = added under this appendix
Note 1: B+M, B+PWD, B+Color Doppler, B+Power Doppler+PWD. B+Power Doppler+PWD Other *: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
Additional Comments:
| Prescription Use | ✓ | AND/OR | Over-The-Counter Use ______ |
|-----------------------------|---|--------|-----------------------------|
| (Part 21 CFR 801 Subpart D) | | | (21 CFR 801 Subpart C) |
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K. K120801
Section 1.3 Indications For Use Page 6 of 15
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System: CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems Transducer: D7C10L Micro-convex Array
| Clinical Application | | | Mode of Operation | | | | | | | |
|---------------------------|---------------------------------|--|-------------------|---|-----|-----|------------------|------------------|----------|-------|
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other |
| Ophthalmic | Ophthalmic | | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | | | | | | | | | |
| | Abdominal | | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | | |
| | Laparoscopic | | | | | | | | | |
| | Pediatric | | | | | | | | | |
| | Small Organ[1] (Specify) | | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | | |
| | Adult Cephalic | | | | | | | | | |
| | Trans- rectal | | | | | | | | | |
| | Trans- vaginal | | N | N | N | | N | N | Note 1 | N |
| | Trans-urethral | | | | | | | | | |
| | Trans- esoph. (non-Card.) | | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | | |
| | Intravascular | | | | | | | | | |
| | Other(Urology) | | N | N | N | | N | N | Note 1 | N |
| | Other (Ob/GYN) | | N | N | N | | N | N | Note 1 | N |
| Cardiac | Cardiac Adult | | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | | |
| | Intra-cardiac | | | | | | | | | |
| | Other (Specify) | | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | | |
| | Other (Specify) | | | | | | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Note 1: B+M. B+PWD, B+Color Doppler, B+Power Doppler, B+Color Doppler+PWD, B+Power Doppler+PWD Other*: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
Additional Comments:
| Prescription Use | <u>✓</u> AND/OR Over-The-Counter Use ______ |
|-----------------------------|---------------------------------------------|
| (Part 21 CFR 801 Subpart D) | (21 CFR 801 Subpart C) |
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
| 510K | K120801 | |
|-------------|---------------------|--------------|
| Section 1.3 | Indications For Use | Page 7 of 15 |
{11}------------------------------------------------
System: CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems Transducer: D6C15L Convex Array
| Clinical Application | | Mode of Operation | | | | | | | |
|----------------------------|---------------------------------|-------------------|---|-----|-----|------------------|------------------|----------|--------|
| General<br>(Track 1. Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | N | N | N | | N | N | Note 1 | N |
| | Abdominal | N | N | N | | N | N | Note 1 | N |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ[1](Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | | | | | | | | |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other(Urology) | N | N | N | | N | N | Note 1 | N |
| | Other (Ob/GYN) | N | N | N | | N | N | Note 1 | N |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | |
| | Other (Specify) | | | | | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
N = new indication; P = previously cleared by FDA; E = added under this appendix
Note 1: B+M, B+PWD, B+Color Doppler, B+Power Doppler+PWD. B+Power Doppler+PWD Other*: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
| Prescription Use <span style="text-decoration: overline;">√</span><br>(Part 21 CFR 801 Subpart D) | AND/OR | Over-The-Counter Use <span style="text-decoration: overline;"></span><br>(21 CFR 801 Subpart C) |
|---------------------------------------------------------------------------------------------------|--------|-------------------------------------------------------------------------------------------------|
|---------------------------------------------------------------------------------------------------|--------|-------------------------------------------------------------------------------------------------|
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
| (Division Sign-Off)<br>Division of Radiological Devices<br>Office of In Vitro Diagnostic Device Evaluation and Safety |
|-----------------------------------------------------------------------------------------------------------------------|
|-----------------------------------------------------------------------------------------------------------------------|
| 510K |
|------|
|------|
Section 1.3
Indications For Use
Page 8 of 15
{12}------------------------------------------------
CHISON iVis 60/ iVis 60EXPERT. Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D7L30L Linear Array
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|----------------------------------------------------------------------------------|-------------------|---|-----|-----|------------------|------------------|----------|--------|
| | | | | | | | | | |
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | | | | | | | | |
| | Abdominal | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ[1] (Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans-esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | N | N | N | | N | N | Note 1 | N |
| | Musculo-skeletal (Superficial) | N | N | N | | N | N | Note 1 | N |
| | Intravascular | | | | | | | | |
| | Other(Urology) | | | | | | | | |
| | Other (Ob/GYN) | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| | N = new indication; P = previously cleared by FDA; E = added under this appendix | | | | | | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
.
.
Note 1: B+M, B+PWD, B+Color Doppler, B+Power Doppler+PWD. B+Power Doppler+PWD. Other *: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
Prescription Use ✓
AND/OR
Over-The-Counter Use __
(Part 21 CFR 801 Subpart D)
(21 CFR 801 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K. K120801
Section 1.3
#### Indications For Use
Page 9 of 15
{13}------------------------------------------------
CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D7L60L Linear Array
| Clinical Application | | Mode of Operation | | | | | | | |
|----------------------|---------------------------------|--------------------------------|---|-----|-----|-------------------------------|---------|----------|--------|
| | | | | | | | | | |
| General | Specific | B | M | PWD | CWD | Color | Power | Combined | Other* |
| (Track 1 Only) | (Tracks 1 & 3) | | | | | Doppler | Doppler | | |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging & | Fetal | | | | | | | | |
| Other | Abdominal | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | N | N | N | | N | N | Note 1 | N |
| | Small Organ[1] (Specify) | N | N | N | | N | N | Note 1 | N |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans- rectal | | | | | | | | |
| | Trans- vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans- esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | N | N | N | | N | N | Note 1 | N |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other(Urology) | | | | | | | | |
| | Other (Ob/GYN) | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | N | N | N | | N | N | Note 1 | N |
| | Other (Specify) | | | | | | | | |
| | N = new indication; | P = previously cleared by FDA; | | | | E = added under this appendix | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Note 1: B+M, B+PWD. B+Color Doppler, B+Power Doppler, B+Color Doppler+PWD. B+Power Doppler+PWD Other *: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
| Prescription Use | ✓ | AND/OR | Over-The-Counter Use |
|-----------------------------|---|------------------------|----------------------|
| (Part 21 CFR 801 Subpart D) | | (21 CFR 801 Subpart C) | |
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
(Division Sign-Off)
Division of Radiological Devices
Office of In Vitro Diagnostic Device Evaluation and Safety
510K. K120801
9
Section 1.3
#### Indications For Use
{14}------------------------------------------------
#### CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems System: Transducer: D7L40L Linear Array
| Clinical Application | | Mode of Operation | | | | | | | |
|---------------------------|-------------------------------------------------------|-------------------|---|-----|-----|-------------------------------|------------------|----------|--------|
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color<br>Doppler | Power<br>Doppler | Combined | Other* |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | | | | | | | | |
| | Abdominal | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | N | N | N | | N | N | Note 1 | N |
| | Small OrganII (Specify) | N | N | N | | N | N | Note 1 | N |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans- rectal | | | | | | | | |
| | Trans- vaginal | | | | | | | | |
| | Trans-urethral | | | | | | | | |
| | Trans- esoph. (non-Card.) | | | | | | | | |
| | Musculo-skeletal (Conventional) | N | N | N | | N | N | Note 1 | N |
| | Musculo-skeletal (Superficial) | | | | | | | | |
| | Intravascular | | | | | | | | |
| | Other(Urology) | | | | | | | | |
| | Other (Ob/GYN) | | | | | | | | |
| Cardiac | Cardiac Adult | | | | | | | | |
| | Cardiac Pediatric | | | | | | | | |
| | Intravascular (Cardiac) | | | | | | | | |
| | Trans-esoph. (Cardiac) | | | | | | | | |
| | Intra-cardiac | | | | | | | | |
| | Other (Specify) | | | | | | | | |
| Peripheral Vessel | Peripheral vessel | N | N | N | | N | N | Note 1 | N |
| | Other (Specify) | | | | | | | | |
| | N = new indication;<br>P = previously cleared by FDA; | | | | | E = added under this appendix | | | |
Intended Use: Diagnostic ultrasound imaging or fluid flow analysis of the human body as follows:
Note 1: B+M. B+PWD, B+Color Doppler, B+Power Doppler, B+Color Doppler+PWD, B+Power Doppler+PWD Other*: Tissue Harmonic Imaging, [1] Small Organ: Thyroid, testes and breast etc.
| Prescription Use<br>(Part 21 CFR 801 Subpart D) | ✓ |
|-------------------------------------------------|---|
| AND/OR | |
| Over-The-Counter Use<br>(21 CFR 801 Subpart C) | |
PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
| (Division Sign-Off)<br>Division of Radiological Devices<br>Office of In Vitro Diagnostic Device Evaluation and Safety<br>510K | K120801 | |
|-------------------------------------------------------------------------------------------------------------------------------|---------------------|---------------|
| Section 1.3 | Indications For Use | Page 11 of 15 |
{15}------------------------------------------------
#### CHISON iVis 60/ iVis 60EXPERT, Q 6/Q8,i7 Diagnostic Ultrasound Systems System: D3P64L Phased Array Transducer:
| Clinical Application | | | Mode of Operation | | | | | | |
|----------------------------------------------------------------------------------|--------------------------------------|---|-------------------|-----|-----|---------------|---------------|----------|--------|
| General<br>(Track 1 Only) | Specific<br>(Tracks 1 & 3) | B | M | PWD | CWD | Color Doppler | Power Doppler | Combined | Other* |
| Ophthalmic | Ophthalmic | | | | | | | | |
| Fetal Imaging &<br>Other | Fetal | | | | | | | | |
| | Abdominal | | | | | | | | |
| | Intra-operative (Specify) | | | | | | | | |
| | Intra-operative (Neuro) | | | | | | | | |
| | Laparoscopic | | | | | | | | |
| | Pediatric | | | | | | | | |
| | Small Organ <sup>(1)</sup> (Specify) | | | | | | | | |
| | Neonatal Cephalic | | | | | | | | |
| | Adult Cephalic | | | | | | | | |
| | Trans-rectal | | | | | | | | |
| | Trans-vaginal | | | | | | | | |
|…
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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.