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FDA 510(k) Applications Submitted by JOHN BLEWITT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K130817
03/25/2013
LTN - LAPAROSCOPIC SURGICAL MESH
LIFECELL CORP.
K161552
06/06/2016
0.9% Sodium Chloride Injection, USP BD PosiFlush SP Syringe
Becton Dickinson and Company
K153481
12/03/2015
0.9% Sodium Chloride Injection, USP BD PosiFlush SF Syringe
BECTON, DICKINSON AND COMPANY
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