# K963808: Choice Powered Wheelchair

- Pathway: 510(k) (Traditional)
- Applicant: American Medical Technology, Inc.
- Decided: Feb 12, 1997 after 142 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 K900330 (1990). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K900330: Quickie P300 Wheelchair, Quickie Designs, Inc. (1990) Summary page 1.
- K940051: Action Storm Power Wheelchair, Invacare Corp. (1994) Summary page 1.
- (no number) EXCELSIOR SR powered wheelchair: named in the summary without a submission number
- (no number) ‘Chairman’ power wheelchair: named in the summary without a submission number

## Most influential descendants
- K031711: Tango, Models, BP1 (2003), 0 descendants of its own

## Indications for use
The CHOICE powered wheelchair is intended to provide mobility for a person who, due to medical reasons, the debilitating nature of some illnesses, because of accident, injury and/or subsequent paralysis, is either missing or unable to use the lower extremities. Some, but not all of the specific indications for use of a power wheelchair are: paraplegia, quadriplegia, ALS, muscular dystrophy, muscular sclerosis, lower limb amputation and any one or more of numerous neurological or muscular diseases which render the limbs too weak or unstable for normal use.

Source page: https://510kreport.com/device/K963808
Methodology: https://510kreport.com/methodology