FDA 510(k) Applications Submitted by KATHRYN B CARR

FDA 510(k) Number Submission Date Device Name Applicant
K090971 04/06/2009 BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY BECTON, DICKINSON & CO.
K081824 06/27/2008 BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) Q AMPLIFIED DNA ASSAY BECTON, DICKINSON & CO.
K081825 06/27/2008 BD PROBETEC NEISSERIA GONORRHOEAE (GC) Q AMPLIFIED DNA ASSAY BECTON, DICKINSON & CO.


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