FDA 510(k) Applications Submitted by ABBOTT VASCULAR-CARDIAC THERAPIES

FDA 510(k) Number	Submission Date	Device Name	Applicant
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
K112957	10/04/2011	HI-TORQUE POWERTURN	ABBOTT VASCULAR-CARDIAC THERAPIES
K103101	10/20/2010	HI-TORQUE BALANCE MIDDLEWEIGHT ELITE	ABBOTT VASCULAR-CARDIAC THERAPIES
K110134	01/18/2011	NC TREK RX CORONARY DILATATION CATHETER	ABBOTT VASCULAR-CARDIAC THERAPIES
K103110	10/08/2010	MINI TREK(TM) RX AND TREK(TM) RX CORONARY DILATATION CATHETER MINI TREK(TM) OTW AND TREK(TM) OTW DILATATION CATHETER	ABBOTT VASCULAR-CARDIAC THERAPIES
K103153	10/14/2010	VOYAGER NC CORONARY DILATATION CATHETER AND NC TREK RX CORONARY DILATATION CATHETER	ABBOTT VASCULAR-CARDIAC THERAPIES