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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