(EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM

(EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM is an FDA 510(k)-cleared medical device (K901840) manufactured by Granbio, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 11, 1990. Regulation: 8.