# Medfusion, Inc.

- Location (FDA's records): Duluth, GA
- FDA decisions: 5 (1989–1991): 5 510(k) clearances
- Product codes: FRN (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medex, Inc.: 2 (https://510kreport.com/company/medex)
- Elixir Corporation: 2 (https://510kreport.com/company/elixir)

## Its most-cited devices
- K901755: Model 3001 Syringe Infusion Pump (1990), cited by 2
- K890120: Syringe Infusion Pump (1989), cited by 2

## Recent decisions
- K905783: Modified Walkmed 400 (Jan 11, 1991)
- K905029: Model 2001, Modification (Dec 24, 1990)
- K901755: Model 3001 Syringe Infusion Pump (Aug 29, 1990)
- K890862: Ambulatory Infusion Pump (Aug 3, 1989)
- K890120: Syringe Infusion Pump (Jul 27, 1989)

Source page: https://510kreport.com/company/medfusion