FDA 510(k) Applications Submitted by AAKASH JAIN

FDA 510(k) Number Submission Date Device Name Applicant
K120600 02/28/2012 DURAGEN SECURE DURAL REGNERATION MATRIX INTEGRA LIFESCIENCES
K160715 03/15/2016 AccuLIF TL and PL Cage STRYKER CORPORATION
K152651 09/16/2015 AccuLIF TL and PL Cage STRYKER CORPORATION
K143616 12/19/2014 AccuLIF TL and PL Cage STRYKER CORPORATION
K163591 12/20/2016 BD PosiFlush Heparin Lock Flush Syringe Becton Dickinson and Company


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