# K133187: FREERIDER FR1, models FR1-13, FR1-15, FR1-17

- Pathway: 510(k) (Traditional)
- Applicant: Freerider Corp
- Decided: Jan 8, 2015 after 448 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: 5 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)
- K092650: Heartway Power Mobility Scooter, S12, Heartway Medical Products Co., Ltd. (2009) Summary page 5.
- K971387: Freerider, Model FR510-F, Freerider USA, Inc. (1997) Summary page 5.

## Indications for use
The device provides transportation for an elderly or disabled person. It can be used in a variety of indoor and outdoor settings.

Source page: https://510kreport.com/device/K133187
Methodology: https://510kreport.com/methodology