# KQS: Table, Cystometric, Non-Electric And Accessories

- Device class: 1; regulation: 21 CFR 876.4890; FDA's rule: 510(k) exempt
- FDA decisions: 8
- 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)
- 1976: 1
- 1979: 1
- 1980: 1
- 1985: 1
- 1986: 2
- 1987: 1
- 1995: 1

## Most-cited predicates
- K955019: Urotract I (1995), cited by 2

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