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Bio-Rad Laboratories, Inc.
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BIOPLEX 2200 EBV IGG PANEL FOR BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM is an FDA 510(k)-cleared medical device (K062211) manufactured by Bio-Rad Laboratories, Inc.. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 7, 2006. Regulation: 8.