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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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