# HNY: Cystotome

- Device class: 1; regulation: 21 CFR 886.4350; FDA's rule: 510(k) exempt
- FDA decisions: 20
- 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)
- 1979: 1
- 1983: 2
- 1984: 4
- 1985: 1
- 1986: 1
- 1987: 3
- 1988: 7
- 1996: 1

## Most-cited predicates

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