# HGH: Cannula, Suction, Uterine

- Device class: 2; regulation: 21 CFR 884.5070; FDA's rule: 510(k) required
- FDA decisions: 6
- 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
- 1994: 1
- 2010: 1
- 2015: 1
- 2017: 1
- 2018: 1

## Most-cited predicates
- K093508: Rigid Cannulae Curved (RC6-RC12), Rigid Cannulae Straight (RS6-RS12) (2010), cited by 1
- K140213: Disposable Endoscopic Cannula (2015), cited by 1

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