FDA 510(k) Applications Submitted by KENNETH WALSH

FDA 510(k) Number Submission Date Device Name Applicant
K120137 01/17/2012 VICTORY GUIDEWIRE (32 MODELS) BRIVANT, LTD.
K140536 03/04/2014 HI TORQUE CONNECT GUIDEWIRE, HI TORQUE CONNECT FLEX GUIDEWIRE, HI TORQUE CONNECT 250T GUIDEWIRE LAKE REGION MEDICAL
K141831 07/07/2014 HYDRAVIEW GUIDEWIRE BRIVANT LIMITED
K122856 09/18/2012 CHARTER GUIDEWIRE BRIVANT, LTD.


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