XYLOSE LYSINE DESOXYCHOLATE AGAR

XYLOSE LYSINE DESOXYCHOLATE AGAR is an FDA 510(k)-cleared medical device (K841131) 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 March 22, 1984. Regulation: 8.