# K261075: Manual Wheelchair (MS01);Manual Wheelchair (MA01)

- Pathway: 510(k) (Traditional)
- Applicant: GuangDong Yong Yi Rehabilitation Equipment Technology Co., Ltd.
- Decided: Jun 22, 2026 after 82 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: 4 generations back to K935398 (1994). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K231750: MA012 Aluminum wheelchair, MS019 steel wheelchair, Sichuan Ast Medical Equipment Co., Ltd. (2023) Summary page 5.

## Indications for use
Manual wheelchair (model:MS01,MA01) is intended for medical purpose to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K261075
Methodology: https://510kreport.com/methodology