MYCOPLASMA PNEUMONIAE ANTIBODY TEST SYSTEM

MYCOPLASMA PNEUMONIAE ANTIBODY TEST SYSTEM is an FDA 510(k)-cleared medical device (K904501) manufactured by Medical Diagnostic Technologies, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 25, 1991. Regulation: 8.