# K071007: Heartway Lightweight Power Mobility Scooter, S33

- Pathway: 510(k) (Traditional)
- Applicant: Heartway Medical Products Co., Ltd.
- Decided: Apr 19, 2007 after 10 days
- Product code: INI (Vehicle, Motorized 3-Wheeled)
- Device class: 2
- Regulation: 21 CFR 890.3800
- 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 K032488 (2003). 1 ancestor in all.
25 later devices descend from it; 2 cite it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032488: Wu's 3-Wheeled Neo Scooter, WT-T3D, Wu'S Tech Co., Ltd. (2003) Summary page 1.

## Most influential descendants
- K101142: Heartway Lightweight Power Mobility Scooter, S34 (2010), 12 descendants of its own
- K072104: Heartway Power Mobility Scooter, PF6 (2007), 11 descendants of its own
- K150987: HEARTWAY Power Mobility Scooter, BRIO S19 (2015), 9 descendants of its own
- K073044: Heartway Power Mobility Scooter, Model PT7 (2007), 6 descendants of its own
- K220227: Auto Folding Scooter, S21F (2022), 5 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/K071007
Methodology: https://510kreport.com/methodology