ANAEROBIC BRUCELLA LAKED BLOOD AGAR

ANAEROBIC BRUCELLA LAKED BLOOD AGAR is an FDA 510(k)-cleared medical device (K791563) manufactured by Anaerobe Systems. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 16, 1979. Regulation: 8.