ACCUPROBE MYCOBACTERIUM INTRACELLULARE CULTURE

ACCUPROBE MYCOBACTERIUM INTRACELLULARE CULTURE is an FDA 510(k)-cleared medical device (K897077) manufactured by Gen-Probe, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 22, 1990. Regulation: 8.