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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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