# Centrimed Corp.

- Location (FDA's records): Hopkins, MN
- FDA decisions: 4 (1984–1985): 4 510(k) clearances
- Product codes: KFM (2), DTQ (2)
- 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
- K851614: Centrimed System 1 W/24 Volt Battery Power Supply (Jun 19, 1985)
- K851615: Centrimed System 1 W/Manual Pump Drive (Jun 19, 1985)
- K851613: Centrimed System 1 W/System 1 Adapter (Jun 19, 1985)
- K842007: Centrimed System 1 (Aug 3, 1984)

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