BACTEC MGIT 960 SYSTEM

BACTEC MGIT 960 SYSTEM is an FDA 510(k)-cleared medical device (K974883) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 30, 1998. Regulation: 8.