# K242791: Electric wheelchair (KR-8807)

- Pathway: 510(k) (Traditional)
- Applicant: Zhejiang Kairui Medical Device Co., Ltd.
- Decided: Nov 12, 2024 after 57 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.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240913: Electric Wheelchair (HBLD3-B); Electric Wheelchair (HBLD3-E), Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd (2024) Summary page 5.

## Most influential descendants
- K250729: Power Wheelchair (MOB1107) (2025), 0 descendants of its own

## Indications for use
It 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/K242791
Methodology: https://510kreport.com/methodology