BD Gets FDA OK for STD Assays | GenomeWeb

NEW YORK (GenomeWeb News) – Becton Dickinson today said that the US Food and Drug Administration has cleared for marketing its BD ProbeTec Chlamydia trachomatis Qx and BD ProbeTec Neisseria gonorrhoeae Qx Amplified DNA Assays with samples collected during women's routine liquid-based Pap testing for cervical cancer screening.

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