# Mediatech, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 24 (1985–1986): 24 510(k) clearances
- Product codes: KIT (23)
- 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
- K860623: Cellgro Hepes Buffer Solution (Mar 3, 1986)
- K854567: Penicillin/Streptomycin Solution (Dec 6, 1985)
- K852603: Mccoy's 5A Medium - Powdered Form (Jul 12, 1985)
- K852485: Cellgro (Iscove's Medium) Modification (Jul 12, 1985)
- K852475: Cellgro Williams' Medium E (Jul 12, 1985)
- K852602: Mccoy's 5A Medium-Liquid Form (Jul 12, 1985)
- K852288: Cellgro (Jun 4, 1985)
- K850510: Emem W/Neaa-Minimum Essential Med. W/Non-Ess. Amin (Mar 4, 1985)

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