K152878 · Danyang Suntec Auto Parts Co., Ltd. · IOR · Feb 3, 2016 · Physical Medicine
Device Facts
Record ID
K152878
Device Name
SUNTEC Mechanical Wheelchair, model ST-WL-1000
Applicant
Danyang Suntec Auto Parts Co., Ltd.
Product Code
IOR · Physical Medicine
Decision Date
Feb 3, 2016
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 890.3850
Device Class
Class 1
Attributes
Therapeutic
Indications for Use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.
Device Story
SUNTEC Mechanical Wheelchair (ST-WL-1000) is a manual, foldable, four-wheeled indoor/outdoor mobility device. It features a sling-style seat and backrest, flip-back armrests, and swing-away detachable elevating footrests. Operated by the user or an attendant, it provides mobility for individuals unable to walk. The device includes a storage pocket, one-button wheel release, and optional seat belt. It is designed for use on standard surfaces; users are advised to avoid sand, wet/icy surfaces, steep inclines (>10 degrees), and escalators. The device is transported by folding the frame and removing components. It assists patients by providing independent or assisted mobility, improving quality of life through increased access to environments.
Clinical Evidence
Bench testing only. The device underwent performance testing in accordance with ISO 7176 series standards, including static stability (ISO 7176-1), brake effectiveness (ISO 7176-3), dimensions/maneuvering (ISO 7176-5), seating dimensions (ISO 7176-7), static/impact/fatigue strength (ISO 7176-8), test dummies (ISO 7176-11), coefficient of friction (ISO 7176-13), information disclosure (ISO 7176-15), ignition resistance (ISO 7176-16), and set-up procedures (ISO 7176-22).
Technological Characteristics
Manual, foldable wheelchair frame. Materials include steel composite handrims and flame-retardant upholstery (CAL 117:2000). Features include PVC solid casters, PU solid rear tires, and manual wheel locks. Dimensions: 31" turning diameter, 2.3" ground clearance. Complies with ISO 7176 series standards for stability, strength, and dimensions. No electronic components or software.
Indications for Use
Indicated for persons restricted to a sitting position requiring mobility assistance. No specific age or gender contraindications provided.
Regulatory Classification
Identification
A mechanical wheelchair is a manually operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position.
{0}------------------------------------------------
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized caduceus symbol, which features a staff with a serpent entwined around it. The logo also includes the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged in a circular pattern around the caduceus symbol.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
February 3, 2016
Danyang Suntec Auto Parts Co., Ltd. Jen Ke-Min Official Correspondent Jiepai Industrial Zone, Jiepai, Danyang Zhenjiang, 212300 CHINA
Re: K152878
Trade/Device Name: SUNTEC Mechanical Wheelchair, Model ST-WL-1000 Regulation Number: 21 CFR 890.3850 Regulation Name: Mechanical Wheelchair Regulatory Class: Class I Product Code: IOR Dated: December 8, 2015 Received: December 16, 2015
Dear Jen Ke-Min:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and 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) that do not require approval of a premarket approval application (PMA). 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. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. 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); medical device reporting (reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in
{1}------------------------------------------------
the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely yours,
# Michael J. Hoffmann -A
for Carlos L. Peña, PhD, MS Director Division of Neurological and Physical Medicine Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
## Indications for Use
510(k) Number (if known) K152878
Device Name
SUNTEC Mechanical Wheelchair, model ST-WL-1000
Indications for Use (Describe)
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.
| Type of Use (Select one or both, as applicable) | |
|-------------------------------------------------|--|
|-------------------------------------------------|--|
Prescription Use (Part 21 CFR 801 Subpart D)
|X | Over-The-Counter Use (21 CFR 801 Subpart C)
#### CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
#### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{3}------------------------------------------------
Image /page/3/Picture/0 description: The image shows the word "SUNTEC" in a blue, sans-serif font. The word is centered within a blue oval. The background is white.
DANYANG SUNTEC AUTO PARTS CO., LTD. Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182 Email:dysuntec@hotmail.com
## SECTION D
510(k) Summary of Safety and Effectiveness
{4}------------------------------------------------
Image /page/4/Picture/0 description: The image contains the word "SUNTEC" in large, bold, dark blue letters. The word is centered inside of a white oval with a dark blue border. The oval is oriented horizontally.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182 Email:dysuntec@hotmail.com
## 510(k) SUMMARY of Safety and Effectiveness
Submitter's Name: DANYANG SUNTEC AUTO PARTS CO., LTD. Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China
| Date Summary Prepared: | January 24, 2016 |
|-------------------------|--------------------------------------------------|
| Proprietary Name: | SUNTEC Mechanical Wheelchair, model ST-WL-1000 |
| Common or Usual Name: | Mechanical Wheelchair |
| Classification Name: | Mechanical Wheelchair, Class I, 21 CFR 890.3850 |
| Product Code: | IOR |
| Official Correspondent: | Dr. Jen, Ke-Min |
| | Email: ceirs.jen@msa.hinet.net |
| | TEL: +886-3-5208829 |
| | FAX: +886-3-5209783 |
| Predicate Device | Valentine International Ltd. |
| | Valentine Steel Wheelchair, model 1000 (K130017) |
Indications For Use: The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.
{5}------------------------------------------------
Image /page/5/Picture/0 description: The image shows the word "SUNTEC" in a bold, dark blue font. The word is enclosed in a dark blue oval. The background of the image is white.
DANYANG SUNTEC AUTO PARTS CO., LTD. Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815
FAX:86-511-86380182 Email:dysuntec@hotmail.com
### Description of the device:
The SUNTEC Mechanical Wheelchair, model ST-WL-1000 is an indoor / outdoor wheelchair that has a base with four-wheeled with a seat. The device can be disassembled for transport and it is foldable easily. The device uses a standard sling type back and seat, and the upholstery fabric meets the Requirements of Section E, Part I for Upholstery Fabrics of California Technical Bulletin CAL 117: 2000 standard for flame retardance.
Following are features for the ST-WL-1000
- Foldable wheelchair frame, lift up backrest handles and strap into place.
- Handy pocket for transporting lightweight items.
- One button easy release wheels.
Due to the features of the body structure, the rear two wheels can always contact the surface, and the vehicle can be operated on the rough surface. But the following surfaces are recommended NOT to operate on:
- Sand surface
- . Wet or icy surface
- . Road maintenance hole metal cover
- Avoid going up multiple steps.
- Avoid using escalators. Use the elevator.
- . Too steep incline over 10 degrees.
- . Turning diameter: 31" / 785 mm
- Ground clearance: 2.3" /58.4 mm
- Curb climbing ability: 0.8" / 20.3 mm
{6}------------------------------------------------
Image /page/6/Picture/0 description: The image shows the word "SUNTEC" in bold, dark blue letters. The word is centered inside a white oval with a dark blue border. The oval is oriented horizontally and takes up most of the frame.
DANYANG SUNTEC AUTO PARTS CO., LTD. Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182
Email:dysuntec@hotmail.com
### Performance Testing:
- 1) ISO 7176-1 Wheelchairs Part 1: Determination of static stability, 1999. (FDA Recognition Number: 16-158 )
- 2) ISO 7176-3 Wheelchairs Part 3: Determination of effectiveness of brakes, 2012. (FDA Recognition Number: 16-192)
- 3) ISO 7176-5 Wheelchairs Part 5: Determination of overall dimensions, mass and maneuvering space, 2008. (FDA Recognition Number: 16-163)
- 4) ISO 7176-7 Wheelchairs Part 7: Determination of seating dimensions Definitions and measuring method, 1998. (FDA Recognition Number: NA)
- 5) ISO 7176-8 Wheelchairs Part 8: Static, impact and fatigue strength for manual wheelchairs, 2014. (FDA Recognition Number: NA)
- 6) ISO 7176-11 Wheelchairs Wheelchairs Part 11: Test dummies, 2012. (FDA Recognition Number: 16-190)
- 7) ISO 7176-13 Wheelchairs Part 13: Determination of coefficient of friction of test surfaces, 1989. (FDA Recognition Number: 16-25)
- 8) ISO 7176-15 Wheelchairs Part 15: Requirements for information disclosure, documentation and labelling, 1996. (FDA Recognition Number: 16-27)
- 9) ISO 7176-16 Wheelchairs Part 16 Requirements and test methods for resistance to ignition of upholstered parts, 2012. (FDA Recognition Number: 16-191)
- 10) ISO 7176-22 Wheelchairs Part 22 Set-up procedures, 2014 (FDA Recognition Number: NA)
{7}------------------------------------------------
Image /page/7/Picture/0 description: The image shows the word "SUNTEC" in a blue, bold, serif font. The word is centered inside a blue oval. The background is white.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182 Email:dysuntec@hotmail.com
### COMPARISON TABLE
| Comparison items | Predicate device<br>(K130017) | Subject device<br>(K152878) | Pose any change in safety or<br>effectiveness, compared with the<br>predicate device? |
|-------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------|
| BRAND NAME | Valentine | SUNTEC | There is no change in safety or<br>effectiveness. |
| MANUFACTURER | Valentine International<br>Ltd. | DANYANG SUNTEC<br>Auto Parts Co., Ltd. | There is no change in safety or<br>effectiveness. |
| MODEL NO | Steel Wheelchair, model<br>1000 | Mechanical Wheelchair,<br>model ST-WL-1000 | There is no change in safety or<br>effectiveness. |
| 510(k) No. | K130017 | K152878 | There is no change in safety or<br>effectiveness. |
| Similarities | | | |
| INTENDED USE | The device is intended<br>for medical purposes to<br>provide mobility to<br>persons restricted to a<br>sitting position. | Same intended use | There is no change in safety or<br>effectiveness. |
| OPERATING<br>ENVIRONMENTS | For Indoor / Outdoor use | Same operating<br>environments | There is no change in safety or<br>effectiveness. |
| TECHNOLOGICAL<br>CHARACTERISTICS | According to ISO<br>7176-1/-3/-5/-7/-8/-11/-1<br>3/ -15/-16 series<br>standards | Same technological<br>characteristics | There is no change in safety or<br>effectiveness. |
| Overall dimensions<br>Length<br>Width<br>Height | 42"<br>25.2"<br>36.2" | Same overall<br>dimensions | There is no change in safety or<br>effectiveness. |
| Seat dimensions<br>Length<br>Height<br>Width | 18"<br>20"<br>18" | 18"<br>20"<br>17.3" - 18.1" | There is no change in safety or<br>effectiveness. |
| FRAME<br>Cross brace<br>Backrest height<br>Reclining backrest<br>Seat sling | YES<br>Un-adjustable<br>fixed<br>Padded Nylon | Same frame | There is no change in safety or<br>effectiveness. |
| ARMREST | | | There is no change in safety or effectiveness. |
| Arm pad | Padded | Same armrest | |
| Flip back | YES, detachable | | |
| Height-adjustable | Pre-installed armrests | | |
| HANGERS | | | There is no change in safety or effectiveness. |
| Swing-away | YES | Same hangers | |
| Elevating leg rest | YES | | |
| Articulating leg rest | YES | | |
| Footplate style | Padded | | |
| Heel loop | No | | |
| Footrest angle | 10~15° | | |
| ACCESSORIES | | | There is no change in safety or effectiveness. |
| Anti-tipper | YES | YES | |
| Fold down push handle | YES | YES | |
| Seat belt | Optional | Optional | |
| REAR AXLE | | | There is no change in safety or effectiveness. |
| Offset axle | YES | Same rear axle | |
| Quick-release axle | YES | | |
| REAR WHEEL | | | There is no change in safety or effectiveness. |
| Size | 24" * 1" | Same size | |
| Tire type | PU Solid Material | Same tire type | |
| Wheel Lock | Pull-to-Lock | Same wheel lock | There is no change in safety or effectiveness. |
| Ground Clearance | 2.3" / 58.4 mm | Same ground clearance | There is no change in safety or effectiveness. |
| Climbing Angle | 10 degrees | Same climbing angle | There is no change in safety or effectiveness. |
| Curb climbing ability | 0.8"/ 20 mm | Same curb climbing ability | There is no change in safety or effectiveness. |
| Minimum turning diameter | 31" / 785 mm | Same turning diameter | There is no change in safety or effectiveness. |
| Differences | | | |
| Weight Capacity | 250 lbs. /113.4 kg | 220 lbs. / 100 kg | The users will maneuver the wheelchair<br>more easily for a lighter wheelchair. |
| Casters | | | PVC material will endure for a longer |
| Size | 8"*1" | Same size | period than PU material. There is no<br>change in safety or effectiveness. |
| Tire type | PU solid material | PVC solid material | |
| Handrim Diameter<br>/material | 22" / Steel Composite | 19.8" / Steel Composite | 10% smaller in handrim diameter is not<br>related for a change in safety or<br>effectiveness. |
| Weight of Chair | 39.6 lb / 18 kg | 38.5 lb / 17.5 kg | 2.7% lighter in total mass will make the<br>user or attendant more easily maneuver<br>the wheelchair. |
| Warranty | | | |
| 12 months for the main parts (footrest, wheel lock, armrest, cross braces, backrest canes, front fork, fork stem house) | 12 months for the main part (footrest, wheel locks, armrest, cross braces, backrest canes, front fork, fork stem house). | The 2 years less guarantee period for chair side frames will make the user pay more money and it is not to do with the change in safety or effectiveness. | |
| The chair side frames are guaranteed 5 years from the date of purchase. | The chair side frames are guaranteed 3 years from the date of purchase. | | |
{8}------------------------------------------------
Image /page/8/Picture/0 description: The image shows the word "SUNTEC" in a dark blue, serif font. The word is centered within a white oval with a thin, dark blue border. The background of the image is white.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182
Email:dysuntec@hotmail.com
{9}------------------------------------------------
Image /page/9/Picture/0 description: The image shows the word "SUNTEC" in a blue, sans-serif font. The word is centered within a blue oval. The background is white.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182
Email:dysuntec@hotmail.com
ISO 7176-5:2008
#### Wheelchairs - Part 5: Determination of overall dimensions, mass and maneuvering space
| Full overall length | 41" / 1050 mm | Same overall length | There is no change in safety or<br>effectiveness. |
|----------------------------------------------------------------------------------------------|-----------------|-------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Overall width | 25" / 640 mm | Same overall width | There is no change in safety or<br>effectiveness. |
| Handgrip height | 36" / 920 mm | 29" / 740 mm | 19.5% lower in handgrip height will<br>cause some uncomforting to a taller<br>person and she/he may bow their waist<br>to hold the wheelchair.<br>As long as the attendant's height is not<br>too large, a normal person will not feel<br>uncomfortable (or to bow his/her waist)<br>to hold the handgrip. There is no<br>change in safety or effectiveness. |
| Stowage length | 42" / 1066 mm | 35.4" / 900 mm | Shorter stowage length means the<br>device can fit the limited width space |
| Stowage width | 11.4" / 290 mm | 14.5" / 370mm | of the more vehicles, leading to more |
| Stowage height | 36.2" / 915 nm | 36.2" / 915 mm | convenience, and larger stowage width<br>means you cannot stack more stuff on<br>the wheelchair. There is nothing to do<br>with the safety and effectiveness<br>concerns. |
| Total mass | 39.6 lb / 18 kg | 38.5 lb / 17.5 kg | 2.7% lighter in total mass will make<br>the user or attendant more easily<br>maneuver the wheelchair. |
| Mass of heaviest part | 39.6 lb / 18 kg | 25.5 lb / 11.7 kg | Lighter mass will make the user or<br>attendant easier to maneuver the<br>wheelchair. |
| Ground clearance | 2.3" / 58.4 mm | Same ground clearance | There is no change in safety or<br>effectiveness. |
| Required width of angled<br>corridor | 35.8" / 910 mm | 34.4" / 875 mm | 3.8% less in angled corridor width has<br>nothing to do with safety or<br>effectiveness. |
| Required doorway entry<br>depth | 52" / 1320 mm | 59" / 1500 mm | 13.6% larger in depth may bring some<br>inconvenience, but we have<br>recommended users to "ALWAYS ASK<br>FOR HELP". There is no change in<br>safety or effectiveness. |
| Required corridor width<br>for side opening | 37.4" / 950 mm | 28.5" / 725 mm | 23.6% narrower in required corridor<br>width will let the user move more<br>easily in the narrower space. |
| ISO 7176-7:1998 | | | |
| Wheelchairs - Part 7: Determination of seating dimensions - Definitions and measuring method | | | |
| Seat plane angle | 3.8° | 4° | 5.3 % larger in seat plane angle cannot<br>pose any change in safety or<br>effectiveness. |
| Effective seat depth | 20"/514 mm | 16.9"/430 mm | 16% less in effective seat depth may<br>bring less free space for adjustment,<br>but there is no change in safety or<br>effectiveness. |
| Seat width | 16.5"/420 mm | 17.3" - 18.1" /<br>440-460 mm | Larger seat width lets users feel more<br>comfortable.<br>There is no change in safety or<br>effectiveness. |
| Effective seat width | 19.3" / 490 mm | 17.3"- 17.5"/<br>440 - 445 mm | Less effective seat width means not to<br>pose a change in safety or<br>effectiveness. |
| Seat surface height at<br>front edge | 19.2"/488 mm | 18.9"/480 mm | 1.6% lower in seat surface height has a<br>negligible difference and will not pose<br>a change in safety or effectiveness. |
| Backrest angle | 8.4° | 10° | 19% larger in backrest angle can bring<br>a more comfortable feeling to the user<br>and there is no change in safety or<br>effectiveness since it passes static and<br>dynamic stabilities tests. |
| Backrest height | 17.2"/439 mm | 16.9"/430 mm | 2% less in backrest height is negligible<br>for posing a change of safety or<br>effectiveness. |
| Backrest width | 16.1"/410 mm | 18.1"/460 mm | 12% larger in backrest width will bring<br>more space for user to load the body.<br>There is no change in safety or<br>effectiveness. |
| Footrest-to-seat | 14.3"/365 mm | 16.5"/420 mm | 15% longer in footrest-to-seat will<br>make the wheelchair easily load a taller<br>person. There is no change in safety or<br>effectiveness. |
| Footrest clearance | 5.8"/148 mm | 6.7"/170 mm | 14.8% higher in footrest clearance will<br>make the wheelchair more easily<br>overcome an obstacle and there is no<br>change in safety or effectiveness. |
| Footrest length | 7.2"/184 mm | 5.9"/150 mm | 18.7% shorter in footrest length will<br>not make a change in safety or<br>effectiveness since 150 mm in footrest<br>length can easily hold a foot of a<br>normal person. |
| Footrest-to-leg angle | 94.6° | 90° | 4.8% smaller in footrest-to-leg angle is<br>negligible to pose a change in safety or<br>effectiveness. |
| | | | effectiveness. |
| Leg-to-seat-surface angle | 91.6° | 97° | 5.8% larger in leg-to-seat-surface angle<br>is negligible to pose a change in safety<br>or effectiveness. |
| Armrest height | 9.5"/242 mm | 10.2"/260 mm | 7.4% larger in armrest height will not<br>pose a change in safety or<br>effectiveness. |
| Front-of-armrest to<br>backrest | 14"/358 mm | 11.4"/290 mm | 18.9% less distance in Front-of-armrest<br>to backrest will let the user feel limited<br>in space but will not pose a change in<br>safety or effectiveness. |
| Armrest length | 10.2"/260 mm | Same length | There is no change in safety or<br>effectiveness. |
| Armrest width | 21.6"/550 mm | Same width | There is no change in safety or<br>effectiveness. |
| Armrest angle | 4.8° | 4° | 16.6% smaller in armrest angle is<br>related to the arm feeling, not related to<br>the safety or effectiveness. |
| Distance between<br>armrests | 18.2"/463 mm | 18.1"/460 mm | 0.64% shorter in distance between<br>armrests does not pose a change in<br>safety or effectiveness. |
| Front location of armrest<br>structure | 13.9"/355 mm | 11"/280 mm | 21% less in front location of armrest<br>structure will not pose a change in<br>safety or effectiveness since 280 mm<br>can provide an enough holding space. |
| Handrim diameter | 21.4"/546 mm | 19.8"/505 mm | 7.6% smaller in Handrim diameter is<br>not related to a change in safety or<br>effectiveness. |
| Propelling wheel<br>diameter | 24"/612 mm | 23.6"/600 mm | 1.9% smaller in propelling wheel<br>diameter has nothing to do with a<br>change in safety or effectiveness. |
| Horizontal location of<br>axle | 2"/53 mm | 1.18"/ 30 mm | 43.4% shorter in Horizontal location of<br>axle has nothing to do with the safety<br>or effectiveness. |
| Vertical location of axle | 3.9"/101 mm | 7"/180 mm | 78% larger in Vertical displacement of<br>wheel axle has nothing to do with the<br>safety or effectiveness. |
| Castor wheel diameter | 7.5"/191 mm | 7.8"/200 mm | 4.7% larger in castor wheel diameter<br>can provide more capability to move<br>on the road, but it is not to pose a<br>change in safety or effectiveness. |
{10}------------------------------------------------
Image /page/10/Picture/0 description: The image shows the word "SUNTEC" in a dark blue, sans-serif font. The word is centered within a white oval shape that is outlined with a thin, dark blue border. The background of the image is white.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182
Email:dysuntec@hotmail.com
{11}------------------------------------------------
Image /page/11/Picture/0 description: The image shows the word "SUNTEC" in a dark blue, sans-serif font. The word is centered inside a white oval with a thin, dark blue border. The oval is oriented horizontally.
Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182
Email:dysuntec@hotmail.com
{12}------------------------------------------------
Image /page/12/Picture/0 description: The image shows the word "SUNTEC" in a bold, dark blue font. The word is centered inside a white oval with a thin, dark blue border. The oval is oriented horizontally.
DANYANG SUNTEC AUTO PARTS CO., LTD. Jiepai Industrial Zone, Jiepai, Danyang, Zhenjiang, Jiangsu Province, 212300 China TEL: 86-511-86380900/ 86370815 FAX:86-511-86380182 Email:dysuntec@hotmail.com
#### COMPARISON DISCUSSION
From the above comparison table, we know that the intended uses of the subject device and the predicate device are the same. Mainframes of two devices are foldable. Removable desk-length armrest and the swing-away detachable elevating footrest are the same. Besides, back upholstery material is the same resistance-ignitability fabric and also meets the requirements for flame retardant. The minor differences in the castor tire type (PU vs. PVC) and the weight of chair (39.6 lb vs. 38.5 lb) do not raise any safety and effectiveness concerns or changes. The tire sizes are indicated on the product durable label. Thus the same safety level for the two devices is assured. At last, the chair side frames are guaranteed for 5 years from the date of purchase for predicate device and 3 years for the subject device. The difference is related with the more cost paid by the user for the chair side frames and does not raise any safety and effectiveness concerns.
Despite of the differences above and shown in the ISO 7176-5: 2008 and ISO 7176-7:1998 comparison table, the subject devices completed the performance tests in accordance with ISO 7176 series standards. They function safely and effectively. There are no safety or effectiveness concerns.
#### CONCLUSIONS
From the comparison table, we know that the subject device is as safe and effective as, and functions in a manner equivalent to the predicate device. The conclusions drawn from the non-clinical tests demonstrate that the device is as effective, and performs as well as the legally marketed device identified in the submission. Thus the subject device is substantially equivalent to the predicate device.
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.