DTM (DERMATOPHYTE TEST MEDIUM) AGAR

DTM (DERMATOPHYTE TEST MEDIUM) AGAR is an FDA 510(k)-cleared medical device (K791414) manufactured by Biomedia, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on October 16, 1979. Regulation: 8.