MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM

MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM is an FDA 510(k)-cleared medical device (K883083) 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 October 24, 1988. Regulation: 8.