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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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