# K253952: Power Wheelchair (OS-R-M01S)

- Pathway: 510(k) (Traditional)
- Applicant: Beijing OrionStar Technology Co., Ltd.
- Decided: Apr 7, 2026 after 118 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The intended use of the powered wheelchair is to provide outdoor and indoor mobility to persons limited to mobility impairment that are capable of operating a powered wheelchair.

Source page: https://510kreport.com/device/K253952
Methodology: https://510kreport.com/methodology