FDA 510(k) Applications Submitted by KATIE COYLE

FDA 510(k) Number Submission Date Device Name Applicant
K151589 06/12/2015 BD MAX CT/GC/TV, BD MAX INSTRUMENT BECTON, DICKINSON, AND COMPANY
K112586 09/06/2011 CEFTAROLINE 30 MICROGRAMS, BBL(TM) SENSI-DISC(TM) BECTON DICKINSON AND COMPANY (BD)
K132909 09/17/2013 BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM TIGECYCLINE (0.25-16 UG/ML) Becton, Dickinson and Company


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