# K100327: Heartway Power Chair, P23

- Pathway: 510(k) (Traditional)
- Applicant: Heartway Medical Products Co., Ltd.
- Decided: Mar 22, 2010 after 46 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 K022697 (2003). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071006: Heartway Attendant-Controlled Power Chair, TC1, Heartway Medical Products Co., Ltd. (2007) Summary page 1.

## Most influential descendants
- K132856: Heartway Power Wheelchair (2014), 0 descendants of its own

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

Source page: https://510kreport.com/device/K100327
Methodology: https://510kreport.com/methodology