# K100824: Mechanical Wheelchair, Model DS 202-S

- Pathway: 510(k) (Traditional)
- Applicant: Suzhou KD Medical
- Decided: May 25, 2010 after 62 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K941989 (1994). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082274: Haida Model HD11 Manual Wheelchair, Jiangyin East China Medical Technology Co., Ltd. (2008)

## Indications for use
DS 202-S manual wheelchair is intended use to provide mobility to physically challenged persons limited to a sitting position on the flat and firm terrain in outdoor and indoor.

Source page: https://510kreport.com/device/K100824
Methodology: https://510kreport.com/methodology