# FIF: Set, Dialysis, Single Needle With Uni-Directional Pump

- Device class: 2; regulation: 21 CFR 876.5820; 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)
- 1977: 1
- 1979: 1
- 1980: 2
- 1982: 1
- 1987: 1

## Most-cited predicates
- K873279: 8810 Pump-Pump Single Needle Device (1987), cited by 1

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