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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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