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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