# MCH: Clip, Hemostatic

- Device class: 2; regulation: 21 CFR 878.4300; FDA's rule: 510(k) required
- FDA decisions: 3
- 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)
- 1990: 1
- 1997: 1
- 2004: 1

## Most-cited predicates
- K040148: Resolution Hemostasis Clipping Device (2004), cited by 3
- K972745: Titanium Hemostatic Clip (1997), cited by 1

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