# K253632: Manual Wheelchair (W50)

- Pathway: 510(k) (Traditional)
- Applicant: Jiangsu Jumao X-Care Medical Equipment Co.,, Ltd.
- Decided: Jan 29, 2026 after 71 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: 3 generations back to K935398 (1994). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K181795: AST Model MA012 and MS019 Rehab Wheelchair, Sichuan Ast Medical Equipment Co., Ltd. (2018) Summary page 5.

## Indications for use
The manual wheelchair is to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K253632
Methodology: https://510kreport.com/methodology