# K982750: Corsaire

- Pathway: 510(k) (Abbreviated)
- Applicant: Optiway, Inc.
- Decided: Feb 1, 1999 after 179 days
- Product code: ITI (Wheelchair, Powered)
- Device class: 2
- Regulation: 21 CFR 890.3860
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K945936 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K945936: JAZZY, Pride Health Care, Inc. (1996) Summary page 3.

## Indications for use
This device is an electric powered wheelchair for indoor use, to be used by partially disabled people capable of operating a few essential hand controls.

Source page: https://510kreport.com/device/K982750
Methodology: https://510kreport.com/methodology