XYLOSE LYSINE DESOXYCHOLATE AGAR

XYLOSE LYSINE DESOXYCHOLATE AGAR is an FDA 510(k)-cleared medical device (K800978) manufactured by Quality Assurance Laboratory, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 27, 1980. Regulation: 8.