# FNG: Lift, Patient, Ac-Powered

- Device class: 2; regulation: 21 CFR 880.5500; FDA's rule: 510(k) exempt
- FDA decisions: 21
- Recalls: 21 (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)
- 1981: 2
- 1985: 3
- 1986: 3
- 1989: 1
- 1990: 3
- 1991: 2
- 1993: 1
- 1994: 2
- 2004: 1
- 2012: 1

## Most-cited predicates
- K041503: Hoverjack Air Patient Lift Device (2004), cited by 1
- K926411: Saf-Lift/Saf-Kary (1993), cited by 1

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