# Sterimed, Inc.

- Location (FDA's records): Acworth, GA
- FDA decisions: 3 (1985–1990): 3 510(k) clearances
- Product codes: KKX (1), DRC (1), IZI (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
- K900664: Disposable Cournand, Seldinger & One-Wall Needles (Jul 18, 1990)
- K863512: Drape Stericover (Sep 30, 1986)
- K853044: Stericover (Nov 1, 1985)

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