# Medix Medical Electronics (U.S.A.), Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1981–1986): 14 510(k) clearances
- Product codes: FRN (5), BZQ (2), FLN (1), FLL (1), BZG (1), CAP (1), CCL (1), BZK (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: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K861040: Enternal Infuser Multipump 203 (Jun 23, 1986)
- K861001: Parenteral Infuser Medipump 204 (Jun 12, 1986)
- K853393: Insulin Pump Insumat 229 (Nov 18, 1985)
- K852433: Infusafe 205 Catolog NO. 205.000 (Jun 27, 1985)
- K813562: Syringe Driver 209 (Feb 1, 1982)
- K812039: Spirometer 210/211 (Sep 25, 1981)
- K812041: Venti-Monitor Model 101 (Sep 25, 1981)
- K812045: Infant Apnea Monitor Model 100 (Sep 24, 1981)

Source page: https://510kreport.com/company/medix-medical-electronics-usa