BIOTIS DECARBOXYLASE MEDIA, ARGININE

BIOTIS DECARBOXYLASE MEDIA, ARGININE is an FDA 510(k)-cleared medical device (K862396) manufactured by Otisville Biotech, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 2, 1986. Regulation: 8.