# KXJ: Table, Radiologic

- Device class: 2; regulation: 21 CFR 892.1980; FDA's rule: 510(k) exempt
- FDA decisions: 31
- 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)
- 1986: 3
- 1987: 2
- 1988: 4
- 1991: 1
- 1992: 1
- 1993: 2
- 1994: 1
- 1995: 3
- 1996: 2
- 2005: 1

## Most-cited predicates
- K940696: Syncra Tilt Option for Angio Diagnost 5 (1994), cited by 1
- K790692: Televix (1979), cited by 1

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