FIAX TEST KIT FOR MYCOPLASMA PNEUMONIAE-G ANTIBODY

FIAX TEST KIT FOR MYCOPLASMA PNEUMONIAE-G ANTIBODY is an FDA 510(k)-cleared medical device (K861716) manufactured by Whittaker Bioproducts, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 7, 1986. Regulation: 8.