FDA 510(k) Applications Submitted by SHIRLEY HYINK

FDA 510(k) Number Submission Date Device Name Applicant
K132099 07/08/2013 ARTHROCARE COBLATOR IQ DLR SPINEWAND, ARTHROCARE COBLATOR IQ DLG SPINEWAND ARTHROCARE CORPORATION
K162074 07/27/2016 Werewolf RF20000 Controller, FLOW 50 Wand ARTHROCARE CORPORATION
K072556 09/10/2007 HEMOSTASIS VALVE MERIT MEDICAL SYSTEMS, INC.
K073035 10/29/2007 PRELUDE AND PRELUDE PRO SHEATH INTRODUCERS MERIT MEDICAL SYSTEMS, INC.


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