# K241588: Electric Wheelchair (KR8803)

- Pathway: 510(k) (Traditional)
- Applicant: Zhejiang Kairui Medical Device Co., Ltd.
- Decided: Nov 25, 2024 after 175 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
Longest line of descent: 6 generations back to K023148 (2003). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232783: Power wheelchair (Model: JMPW-01W), Jiangsu Jumao X-Care Medical Equipment Co., Ltd. (2024) Summary page 6.

## Indications for use
The "Electric Wheelchair, Model: KR8803" is a motor driven, indoor and outdoor transportation vehicle with the intended use to provide mobility to a disabled or elderly person limited to a seated position.

Source page: https://510kreport.com/device/K241588
Methodology: https://510kreport.com/methodology