Bio-Rad Laboratories Inc., Clinical Systems Divisi
Bio-Rad Laboratories Inc., Clinical Systems Divisi holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2008.
Top product codes for Bio-Rad Laboratories Inc., Clinical Systems Divisi
Recent clearances by Bio-Rad Laboratories Inc., Clinical Systems Divisi
- K080911 — VARIANT NBS SICKLE CELL PROGRAM REAGENT KIT, VARIANT NBS NEWBORN SCREENING SYSTEM AND VARIANT NBS WORKSTATION WITH
- K070819 — VARIANT II TURBO LINK HEMOGLOBIN A1C PROGRAM, AND VARIANT II TURBO LINK HEMOGLOBIN TESTING WITH MODEL, 270-2716,
- K063643 — MODIFICATION TO VARIANT II: HEMOGLOBIN A1C PROGRAM, BETA-THALASSEMIA SHORT PROGRAM AND TOTAL GHB PROGRAM
Data sourced from openFDA. This site is unofficial and independent of the FDA.