# K163204: A08 Power wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Kunshan Aoshida Electric Technology Co., Ltd.
- Decided: May 5, 2017 after 171 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.
7 later devices descend from it; 5 cite it directly.
0 of 12 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 4.

## Most influential descendants
- K241529: Powered Wheelchair (NXN20-209) (2024), 1 descendant of its own
- K232783: Power wheelchair (Model: JMPW-01W) (2024), 1 descendant of its own
- K252862: Electric Wheelchair (DH01126) (2025), 0 descendants of its own
- K241588: Electric Wheelchair (KR8803) (2024), 0 descendants of its own
- K241603: Powered Wheelchair (NXN20-208, NXN20-211) (2024), 0 descendants of its own

## Indications for use
The device 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/K163204
Methodology: https://510kreport.com/methodology