# K963385: Quickie Power Wheelchairs P200 Series

- Pathway: 510(k) (Traditional)
- Applicant: Quickie Designs, Inc.
- Decided: Apr 28, 1997 after 244 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
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. The FDA summary names its predicate without a number.
- (no number) Quickie P100: named in the summary without a submission number
- (no number) Quickie P110: named in the summary without a submission number
- (no number) Quickie P190: named in the summary without a submission number
- (no number) Quickie P500: named in the summary without a submission number
- (no number) Quickie P200: named in the summary without a submission number
- (no number) Quickie P210: named in the summary without a submission number
- (no number) Quickie P320: named in the summary without a submission number
- (no number) Quickie P300: named in the summary without a submission number
- (no number) Everest and Jennings Lancer 2000: named in the summary without a submission number
- (no number) Everest and Jennings Sabre: named in the summary without a submission number
- (no number) Everest and Jennings Sabre ES: named in the summary without a submission number
- (no number) Pride Health Care Inc. Jazzy: named in the summary without a submission number

## Indications for use
Quickie Powered Wheelchairs empower physically challenged persons by providing a means of mobility.

Source page: https://510kreport.com/device/K963385
Methodology: https://510kreport.com/methodology