MYCOPLASMA PNEUMONIAE ANTIBODY EIA TEST SYSTEM

MYCOPLASMA PNEUMONIAE ANTIBODY EIA TEST SYSTEM is an FDA 510(k)-cleared medical device (K920212) manufactured by Shared Systems, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 19, 1992. Regulation: 8.