FDA 510(k) Applications Submitted by FRED L BOUCHER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K974713	12/17/1997	BARD HYDROPHILLIC COATED GUIDE WIRE	C.R. BARD, INC.
K030201	01/21/2003	MODIFICATION TO EXPORT ASPIRATION CATHETER	MEDTRONIC VASCULAR
K050139	01/21/2005	MODIFICATION TO: EXPORT CATHETER	MEDTRONIC VASCULAR
K010579	02/27/2001	STENT SUPPORT GUIDE CATHETER	MEDTRONIC VASCULAR
K000677	02/29/2000	ZUMA GUIDE CATHETERS	MEDTRONIC VASCULAR
K030671	03/03/2003	MEDTRONIOC 7F LAUNCHER BIOPSY GUIDE CATHETER, MODEL LA7RVBB, MEDTRONIC 8F LAUNCHER BIOPSY CATHETER, MODEL LA8RVBB	MEDTRONIC VASCULAR
K030779	03/11/2003	5F MEDTRONIC LAUNCHER GUIDE CATHETER	MEDTRONIC VASCULAR
K040869	04/02/2004	EXPORT CATHETER	MEDTRONIC VASCULAR
K021256	04/19/2002	Z3 GUIDE CATHETER	MEDTRONIC VASCULAR
K001969	06/28/2000	GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300	MEDTRONIC VASCULAR
K992237	07/02/1999	MEDTRONIC GT2 FUSION GUIDE WIRES	MEDTRONIC VASCULAR
K051846	07/07/2005	7F SHERPA NX GUIDE CATHETER	MEDTRONIC VASCULAR
K022764	08/21/2002	7F LAUNCHER GUIDE CATHETER	MEDTRONIC VASCULAR
K042489	09/14/2004	6F Z4 GUIDE CATHETER	MEDTRONIC VASCULAR
K023303	10/03/2002	EXPORT ASPIRATION CATHETER	MEDTRONIC VASCULAR
K023402	10/10/2002	8F LAUNCHER GUIDE CATHETER	MEDTRONIC VASCULAR
K023878	11/21/2002	GUARDWIRE TEMPORARY OCCLUSION AND ASPIRATION SYSTEM	MEDTRONIC VASCULAR