INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCA

INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCA is an FDA 510(k)-cleared medical device (K864347) 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 February 1, 1987. Regulation: 8.