(14 days)
Not Found
No
The description explicitly states it is a "manually operated mechanical wheelchair" and lists components typical of manual wheelchairs. There is no mention of AI, ML, or any computational processing.
No
Explanation: The device description clearly states it is a "manually operated mechanical wheelchair" that provides "enhanced mobility to physically challenged persons." This indicates it is for supportive mobility, not for treating a disease or condition. Its predicate device is also a manual wheelchair.
No
The provided text describes a manual mechanical wheelchair, whose purpose is to provide mobility. There is no mention of it being used to diagnose any condition or disease.
No
The device description clearly states it is a "manually operated mechanical wheelchair" and describes physical components like wheels and a folding frame, indicating it is a hardware device.
No, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD definition: In Vitro Diagnostics are medical devices used to examine specimens taken from the human body (like blood, urine, or tissue) to provide information about a person's health.
- Device description: The provided information clearly describes a manual wheelchair. Its purpose is to provide mobility to individuals with physical limitations. It does not involve the analysis of any biological specimens.
The description of the device and its intended use are entirely focused on mechanical support and mobility, which are not functions of an IVD.
N/A
Intended Use / Indications for Use
The FS-series Wheelchair is manually operated mechanical wheelchair, the FS-series Wheelchair provides enhanced mobility to physically challenged persons limited to a sitting position
Product codes
IOR
Device Description
Foshan Wheelchair is a self-propelled, folding frame, mechanical wheelchair consisting of components typical of most manual wheelchairs. It has large rear wheels with push rims for self-propulsion and small front pivoting casters for turning and stability. It is a lightweight, user adaptable, everyday chair for use both indoors and outdoors.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 890.3850 Mechanical wheelchair.
(a)
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.(b)
Classification. Class I (general controls).
0
| 510(K)Summary | K0418 | |
|---|---|---|
| JUL 2 0 2004 | ||
| Submitter's Name: | Foshan Dongfang Medical Equipment Manufactory (LTD.) | |
| Address: | 2 Baohua Industrial Park Ave. Guilan Rd. Nanhai District Foshan City, | |
| Guangdong Province, China ,528252 | ||
| Telephone: | ||
| Fax: | 86-757-6299415 | |
| 86-757-6232649 | ||
| Contact: | ||
| Date Prepared: | Mr. Pang Jianxun , General Manager |
FS Wheelchair Device Name: L
- FS Wheelchair is classified under Mechanical Wheelchair, which 3. Classification: has been classified as a Class I device, in accordance to 21 code of Federal Regulations 890.3850
- Foshan Machinery & Equipment Import & Export Co. Series Wheel 4. Predicate Device: Chair (manual, not electrical)
- Device Description:
Foshan Wheelchair is a self-propelled, folding frame, mechanical wheelchair consisting of components typical of most manual wheelchairs. It has large rear wheels with push rims for self-propulsion and small front pivoting casters for turning and stability. It is a lightweight, user adaptable, everyday chair for use both indoors and outdoors.
- Intended Use
The intended used Foshan Wheelchair is to provide mobility to persons with physical limitations limited to a sitting position.
- Substantial Equivalence
The Foshan Wheelchair is substantially equivalent to the listed predicate devices in its specifications, performance and use.
1
Image /page/1/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal is circular and contains the department's name around the perimeter. In the center of the seal is an abstract image of an eagle with three lines representing its wings. The eagle is facing to the right.
Public Health Service
JUL 2 0 2004
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
Foshan Dongfang Medical Equipment Manufactory C/o Mr. Tamas Borsai TUV Rheinland of North America, Inc. 12 Commerce Road Newtown, Connecticut 06470
Re: K041814
Trade/Device Name: FS-Series Wheelchair Regulation Number: 21 CFR 890.3850 Regulation Name: Mechanical wheelchair Regulatory Class: I Product Code: IOR Dated: June 28, 2004 Received: July 6, 2004
Dear Mr. Borsai:
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.
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 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); 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.
2
Page 2 - Mr. Tamas Borsai
This letter will allow you to begin marketing your device as described in your Section 510(k) This letter will anow yourse ough finding of substantial equivalence of your device to a legally premailed predicate device results in a classification for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please If you desire specific at (301) 594-4659. Also, please note the regulation entitled, Colliable of Compulance in (set notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small other general international and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely yours,
Mark A. Milburn
Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
Indications for Use
510 (K) Number (if known) : Under application
Device Name: FS-Series Wheelchair
Indications For Use:
The FS-series Wheelchair is manually operated mechanical wheelchair, the FS-series Wheelchair provides enhanced mobility to physically challenged persons limited to a sitting position
Prescription Use______________________________________________________________________________________________________________________________________________________________
AND/OR
0ver-The-Counter Use
(Part 21 CFR 801 Subpart D)
(21 CFR 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Mark A. Milkersen
(Division Sign-Off) Division of General, Restorative, and Neurological Devices
510(k) Number K041814