BARTELS EPSTEIN-BARR VIRUS IGM EIA

BARTELS EPSTEIN-BARR VIRUS IGM EIA is an FDA 510(k)-cleared medical device (K922331) manufactured by Baxter Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 1, 1992. Regulation: 8.