# K234098: Mobility Scooter (C4+)

- Pathway: 510(k) (Traditional)
- Applicant: Yongkang Yile Vehicle Co., Ltd.
- Decided: Apr 18, 2024 after 114 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: 6 generations back to K032488 (2003). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132855: Heartway Power Mobility Scooter, Heartway Medical Products Co., Ltd. (2014) Summary page 5.

## Indications for use
The mobility scooter is intended for providing assistance to people restricted to a sitting position.

Source page: https://510kreport.com/device/K234098
Methodology: https://510kreport.com/methodology