# FIQ: Cannula, A-V Shunt

- Device class: 2; regulation: 21 CFR 876.5540; FDA's rule: 510(k) required
- FDA decisions: 23
- 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)
- 1977: 1
- 1978: 1
- 1979: 1
- 1980: 1
- 1981: 4
- 1982: 1
- 1983: 5
- 1984: 5
- 1985: 1
- 1989: 3

## Most-cited predicates

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