# KNO: Accessories, Wheelchair

- Device class: 1; regulation: 21 CFR 890.3910; FDA's rule: 510(k) exempt
- FDA decisions: 35
- Recalls: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1976: 4
- 1978: 8
- 1979: 2
- 1980: 4
- 1981: 6
- 1982: 7
- 1983: 3
- 1987: 1

## Most-cited predicates
- K823816: Wheelchair Patient Restraints (1983), cited by 1

Source page: https://510kreport.com/product-code/KNO
Data by year (CSV): https://510kreport.com/product-code/KNO.csv