# K250366: Electric Wheelchair (LW01301A07)

- Pathway: 510(k) (Traditional)
- Applicant: Anhui Longway Medical Technology Co., Ltd.
- Decided: Apr 8, 2025 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: 5 generations back to K023148 (2003). 5 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K220747: Power Wheelchair (N5515B), Zhejiang Innuovo Rehabilitation Devices Co.,Ltd (2022) Summary page 6.

## Most influential descendants
- K260937: Smart Electric Wheelchair (R1-Std-BK, R1-Pro-BK, R1-Ultra-GK, R1-Ultra-WK) (2026), 0 descendants of its own
- K254012: Electric Wheelchair (E201) (2026), 0 descendants of its own
- K253599: Electric Wheelchair (W-A807, W-A807L) (2026), 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/K250366
Methodology: https://510kreport.com/methodology