XYLOSE LYSINE DEOXYCHOLATE AGAR

XYLOSE LYSINE DEOXYCHOLATE AGAR is an FDA 510(k)-cleared medical device (K811604) 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 June 24, 1981. Regulation: 8.