# Med Fusion Systems, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 22 (1977–1987): 22 510(k) clearances
- Product codes: FPA (5), ITQ (4), FNJ (3), FRN (2), LDQ (2), FMI (1), DYB (1), IPS (1), FPB (1), FMF (1), FSM (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K873961: Infumed 300 Ambulatory Infusion Pump (Dec 29, 1987)
- K870524: Ambulatory Infusion Pump Drug Reservoir (May 6, 1987)
- K870907: Introducer, Percutaneous (Apr 9, 1987)
- K864407: Refillable Syringe (Jan 20, 1987)
- K863814: Bag Spike Extension Set (Oct 14, 1986)
- K860616: Volume Control Set with Extension (Jun 2, 1986)
- K860803: IV Filter Extension Set (Apr 9, 1986)
- K844313: Infuset W/Huber Needle (Jan 22, 1985)

Source page: https://510kreport.com/company/med-fusion-systems