FDA 510(k) Applications Submitted by SUZANNE REDMAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110134	01/18/2011	NC TREK RX CORONARY DILATATION CATHETER	ABBOTT VASCULAR-CARDIAC THERAPIES
K110617	03/03/2011	MINI TREK RX 1.20 MM CORONARY DILATATION CATHETER, MINI TREK OTW 1.20 MM CORONARY DILATATION CATHETER	Abbott Vascular
K121222	04/23/2012	TREK OTW CORONARY DILATATION CATHETER MINI TREK OTW CORONARY DILATATION CATHETER	Abbott Vascular
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
K123279	10/22/2012	MINI TREK RX CORONARY DILATATION CATHETER (INCLUDING 1.20 MM SIZE), MINI TREK OTW CORONARY DILATATION CATHETER (INCLUDIN	Abbott Vascular
K113464	11/22/2011	NC TREK OTW CORONARY DILATATION CATHETER	Abbott Vascular