# FPP: Stretcher, Hand-Carried

- Device class: 1; regulation: 21 CFR 880.6900; FDA's rule: 510(k) exempt
- FDA decisions: 39
- Recalls: 12 (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)
- 1985: 1
- 1986: 1
- 1987: 3
- 1989: 2
- 1990: 10
- 1991: 5
- 1992: 3
- 1993: 3
- 1994: 3
- 2003: 1

## Most-cited predicates
- K902521: Weevac 6 Infant Evacuation Stretcher (1990), cited by 1

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