BACTEC 13A MEDIUM (7H13)

BACTEC 13A MEDIUM (7H13) is an FDA 510(k)-cleared medical device (K863191) 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 September 14, 1986. Regulation: 8.