# KYX: Dispenser, Liquid Medication

- Device class: 1; regulation: 21 CFR 880.6430; FDA's rule: 510(k) exempt
- FDA decisions: 11
- Recalls: 4 (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)
- 1976: 1
- 1977: 1
- 1978: 1
- 1979: 1
- 1980: 3
- 1983: 1
- 1995: 1
- 1998: 1
- 2015: 1

## Most-cited predicates
- K792227: Multi-AD Fluid Dispensing System (1979), cited by 3
- K980109: Cyclotech Cyclosporine Oral Solutions Dispenser (1998), cited by 1
- K801008: Multi-AD Fluid Dispensing Pump MP-3000 (1980), cited by 1

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