
Bio-Rad Laboratories, Inc.
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ACCESS(R) CHLAMYDIA EIA AND BLOCKING ASSAY is an FDA 510(k)-cleared medical device (K935807) 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 May 18, 1995. Regulation: 8.

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