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Becton, Dickinson & CO
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BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) Q AMPLIFIED DNA ASSAY is an FDA 510(k)-cleared medical device (K091724) manufactured by Becton, Dickinson & CO. This device is classified under the Microbiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 12, 2009. Regulation: 8.