# Medix Corp.

- Location (FDA's records): Le17 6db, England, GB
- FDA decisions: 6 (1978–2004): 6 510(k) clearances
- Names in FDA's records: Medix Corp. (5); Medix, Inc. (1)
- Product codes: CAF (2), GZJ (1), FRN (1), FOZ (1), CCQ (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
- K041345: Protectiv Jelco Safety I.V. Catheter, Model 3600 Series (Jul 22, 2004)
- K921273: Easimist Ultrasonic Nebulizer (Apr 1, 1994)
- K914772: Medix Nebulizing System Code NO. 2000 and 2001 (Jul 24, 1992)
- K853071: Medix Electronic Nebulizing System (Aug 29, 1985)
- K822454: Syringe Pump 209-100 (Oct 18, 1982)
- K780444: Nervtron-RX (Apr 19, 1978)

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