ACCUPROBE MYCOBACTERIUM GORDONAE CULTURE TEST

ACCUPROBE MYCOBACTERIUM GORDONAE CULTURE TEST is an FDA 510(k)-cleared medical device (K896492) 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 April 15, 1990. Regulation: 8.