# K254141: Manual Wheelchair (DY01903(2))

- Pathway: 510(k) (Traditional)
- Applicant: Guangdong Dayang Medical Technology Co., Ltd.
- Decided: May 21, 2026 after 150 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: 1 generation back to K242560 (2024). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242560: Manual Wheelchair (SYIV100-CA9221), Foshan Shunkangda Medical Tech Co., Ltd. (2024) Summary page 5.

## Indications for use
The DY01903(2)) Manual Wheelchair is to provide mobility to persons limited to a sitting position.

Source page: https://510kreport.com/device/K254141
Methodology: https://510kreport.com/methodology