# K061810: Cougar Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: R82 A/S
- Decided: Aug 7, 2006 after 41 days
- Product code: IOR (Wheelchair, Mechanical)
- Device class: 1
- Regulation: 21 CFR 890.3850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Cougar Wheelchair's intended function and use is to provide mobility to persons limited to a sifting position. The wheelchair consists primarily of an aluminum frame, large rear wheels with hand rims for propelling the wheelchair or smaller rear wheels for attendant-only use, and smaller front pivoting casters for steering and turning.

Source page: https://510kreport.com/device/K061810
Methodology: https://510kreport.com/methodology