# MOV: Catheters, Salpingography

- Device class: 2; regulation: 21 CFR 884.4530; FDA's rule: 510(k) required
- FDA decisions: 5
- Recalls: 2 (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)
- 1995: 4
- 2018: 1

## Most-cited predicates
- K931476: Novy Cornual Cannulation Set (1995), cited by 1

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