CYSTINE TRYPTIC AGAR W/MANNITOL

CYSTINE TRYPTIC AGAR W/MANNITOL is an FDA 510(k)-cleared medical device (K844545) manufactured by bioMerieux, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 15, 1985. Regulation: 8.