Bio-Rad Laboratories, Inc., Clinical Systems Divis is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bio-Rad Laboratories, Inc., Clinical Systems Divis - FDA 510(k) Clear...
Recent clearances: VARIANT(TM) II TURBO HBA1C KIT - 2.0, VARIANT II HEMOGLOBIN A1C PROGRAM (NEW), VARIANT II HEMOGLOBIN TESTING SYSTEM WITH CDM SOFTWARE, CDM SOFTWARE, VARIANT II TURBO HBA1C KIT-2.0 VARIANT II TURBO HEMOGLOBIN TESTING SYSTEM
3
Total
3
Cleared
0
Denied
Bio-Rad Laboratories, Inc., Clinical Systems Divis has 3 FDA 510(k) cleared medical devices. Based in Hercules, US.
Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Bio-Rad Laboratories, Inc., Clinical Systems Divis Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bio-Rad Laboratories, Inc., Clinical Systems Divis
3 devices