MYCOAKT M KANSASII CULTURE ID KIT

MYCOAKT M KANSASII CULTURE ID KIT is an FDA 510(k)-cleared medical device (K943050) manufactured by Dynagen, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 12, 1995. Regulation: 8.