FDA 510(k) Applications Submitted by KAY SETZER

FDA 510(k) Number Submission Date Device Name Applicant
K101011 04/12/2010 HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL ABBOTT VASCULAR INC.
K101116 04/21/2010 HI-TORQUE PILOT 50 AND 150 GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER LS AND MS GUIDE WIRE WITH ABBOTT VASCULAR-CARDIAC THERAPIES
K122573 08/23/2012 HI-TORQUE COMMAND GUIDE WIRE FAMILY ABBOTT VASCULAR INC.
K112957 10/05/2011 HI-TORQUE POWERTURN ABBOTT VASCULAR-CARDIAC THERAPIES
K103101 10/21/2010 HI-TORQUE BALANCE MIDDLEWEIGHT ELITE ABBOTT VASCULAR-CARDIAC THERAPIES


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