Greiner America, Inc.
Greiner America, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 1997.
Top product codes for Greiner America, Inc.
Recent clearances by Greiner America, Inc.
- K971220 — GREINER VACUETTE BLOOD COLLECTION TUBE
- K971236 — GREINER VACUETTE BLOOD COLLECTION TUBE
- K971239 — GREINER VACUETTE BLOOD COLLECTION TUBE
- K971221 — GREINER VACUETTE BLOOD COLLECTION TUBE
- K960860 — GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3
- K960857 — GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR
- K960858 — GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.