# K972797: Tool-Less Wheel Chair

- Pathway: 510(k) (Traditional)
- Applicant: Sunrise Medical, Inc.
- Decided: Aug 12, 1997 after 15 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. The FDA summary names its predicate without a number.
- (no number) Quickie’s GPS: named in the summary without a submission number
- (no number) Invacare’s A-4: named in the summary without a submission number
- (no number) Everest & Jennings’ Barracuda: named in the summary without a submission number

## Indications for use
Quickie manual wheelchairs empower physically challenged persons by providing a means of mobility. This includes temporary and permanent conditions in all ages such as: Arthritis Tetraplegic Multiple Sclerosis Amputee Quadriplegic Polio Paraplegic Spina Bifida Geriatric conditions Cerebral Palsy Head Injury or Trauma And other immobilizing or debilitating condition Hemiplegic Muscular Dystrophy

Source page: https://510kreport.com/device/K972797
Methodology: https://510kreport.com/methodology