# FRZ: Device, Patient Transfer, Powered

- Device class: 2; regulation: 21 CFR 880.6775; FDA's rule: 510(k) exempt
- FDA decisions: 5
- Recalls: 1 (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)
- 1984: 3
- 1992: 1
- 2013: 1

## Most-cited predicates
- K121929: Zephyr 'X-Series Patient Transfer Sled (2013), cited by 1

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