# K073044: Heartway Power Mobility Scooter, Model PT7

- Pathway: 510(k) (Traditional)
- Applicant: Heartway Medical Products Co., Ltd.
- Decided: Dec 7, 2007 after 39 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: 3 generations back to K032488 (2003). 3 ancestors in all.
6 later devices descend from it; 3 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072104: Heartway Power Mobility Scooter, PF6, Heartway Medical Products Co., Ltd. (2007) Summary page 1.

## Most influential descendants
- K092650: Heartway Power Mobility Scooter, S12 (2009), 3 descendants of its own
- K132855: Heartway Power Mobility Scooter (2014), 1 descendant of its own
- K234098: Mobility Scooter (C4+) (2024), 0 descendants of its own
- K133187: FREERIDER FR1, models FR1-13, FR1-15, FR1-17 (2015), 0 descendants of its own
- K092155: Heartway Power Mobility Scooter, S8 (2009), 0 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/K073044
Methodology: https://510kreport.com/methodology