# Chronimed, Inc.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 5 (1997–2001): 5 510(k) clearances
- Product codes: CGA (2), JJX (1), LJX (1), NBW (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Genesis Labs, Inc.: 2 (https://510kreport.com/company/genesis-labs)

## Recent decisions
- K010039: Quicktek Blood Glucose System, Quicktek Blood Glucose Meter, Quicktek Blood Glucose Strips, Quicktek Control Solution (Aug 10, 2001)
- K983432: Supreme II Control Solutions (Dec 17, 1998)
- K980573: Sensorex Blood Glucose Monitoring System (Jul 30, 1998)
- K981555: Diascreen Reagent Strips (Jun 1, 1998)
- K963544: Supreme II Meter (Feb 20, 1997)

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