Roche Diagnostics/Boehringer Mannheim GmbH
Roche Diagnostics/Boehringer Mannheim GmbH holds FDA 510(k) medical device clearances, first cleared 1998, most recent 1999.
Top product codes for Roche Diagnostics/Boehringer Mannheim GmbH
Recent clearances by Roche Diagnostics/Boehringer Mannheim GmbH
- K983892 — COAGUCHEK PRO SYSTEM, APTT TEST CARTRIDGES FOR COAGUCHEK PRO SYSTEM, APTT CONTROLS FOR COAGUCHEK PRO SYSTEM, COAGUCHEK P
- K981931 — CEDIA RED BLOOD CELL FOLATE REAGENT PACK, CEDIA FOLATE ASSAY AND ELECSYS FOLATE ASSAY
- K981632 — ROCHE DIAGNOSTICS, BOEHRINGER MANNHEIM LIQUID TOTAL BILIRUBIN REAGENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.