NEOMYCIN BLOOD AGAR

NEOMYCIN BLOOD AGAR is an FDA 510(k)-cleared medical device (K843492) 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 October 1, 1984. Regulation: 8.