KANAMYCIN-VANCOMYCIN-LAKED BLOOD AGAR

KANAMYCIN-VANCOMYCIN-LAKED BLOOD AGAR is an FDA 510(k)-cleared medical device (K851347) manufactured by Micro Media Laboratories. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 18, 1985. Regulation: 8.