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FDA 510(k) Applications Submitted by SHERMA WINSTON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140446
02/21/2014
BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY
BECTON, DICKINSON & CO.
K140447
02/21/2014
BD VIPER LT SYSTEM
Becton, Dickinson and Company
K140448
02/21/2014
BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY
BECTON, DICKINSON & CO.
K120728
03/09/2012
PHASIX PLUG AND PATCH
C.R. BARD INC
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