# K043435: Quickie Interchange FWD W/Lift Power Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical
- Decided: Feb 11, 2005 after 60 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: 3 generations back to K900565 (1990). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K991168: Arrow FWD Power Wheelchair, Invacare Corp. (1999) Summary page 1.

## Indications for use
The Quickie Interchange FWD w/ Lift Power Wheelchair's intended use is to empower physically challenged individuals by providing a means of mobility.

Source page: https://510kreport.com/device/K043435
Methodology: https://510kreport.com/methodology