FDA 510(k) Applications Submitted by JANINE SPAFFORD

FDA 510(k) Number Submission Date Device Name Applicant
K100722 03/15/2010 TELAVANCIN 30 UG, BBL SENSI-DISC Becton, Dickinson and Company
K191964 07/23/2019 BD Kiestra IdentifA Becton, Dickinson and Company


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