# K062888: Middle Wheel Drive Power Chair, CWD01

- Pathway: 510(k) (Traditional)
- Applicant: Emg Technology Co., Ltd.
- Decided: Oct 24, 2006 after 28 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: 1 generation back to K023148 (2003). 1 ancestor in all.
78 later devices descend from it; 5 cite it directly.
0 of 80 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023148: Epw Powered Wheelchair, GP-201, Emg Technology Co., Ltd. (2003) Summary page 1.

## Most influential descendants
- K070501: Ruike 3421 Powered Wheelchair (2007), 73 descendants of its own
- K113463: Power Wheelchair (2012), 71 descendants of its own
- K220747: Power Wheelchair (N5515B) (2022), 37 descendants of its own
- K231508: Power Wheelchair, W5521 (2023), 8 descendants of its own
- K230964: Power Wheelchair (N5909) (2023), 7 descendants of its own

## Indications for use
The device is intended for medical purposes to provide mobility to persons restricted to a sitting position.

Source page: https://510kreport.com/device/K062888
Methodology: https://510kreport.com/methodology