# K261078: Electric Scooter (FNS01,FNS03)

- Pathway: 510(k) (Traditional)
- Applicant: Anhui Jbh Medical Apparatus Co., Ltd.
- Decided: Sep 24, 2026 after 176 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: 7 generations back to K032488 (2003). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252349: Electric Scooter (Mojo-T330), Dongguan Smarfody Mobility Technology Co., Ltd. (2026) Summary page 5.

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

Source page: https://510kreport.com/device/K261078
Methodology: https://510kreport.com/methodology