# KPX: Changer, Radiographic Film/Cassette

- Device class: 2; regulation: 21 CFR 892.1860; FDA's rule: 510(k) exempt
- FDA decisions: 26
- Recalls: 0 (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: 1
- 1985: 2
- 1986: 1
- 1987: 1
- 1990: 2
- 1991: 1
- 1992: 3
- 1993: 4
- 1994: 1
- 1995: 1

## Most-cited predicates
- K800751: Radx Vent-AL Mechanical Resporator (1980), cited by 1

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