# K262241: Electric Wheelchair (0080)

- Pathway: 510(k) (Traditional)
- Applicant: Xuzhou Heabens Medical Technology Co., Ltd.
- Decided: Sep 29, 2026 after 90 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: 4 generations back to K023148 (2003). 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)
- K113463: Power Wheelchair, Suzhou KD Medical Appliance Co., Ltd. (2012) Summary page 5.

## Indications for use
The electric wheelchair 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/K262241
Methodology: https://510kreport.com/methodology