FDA 510(k) Applications Submitted by JENNIFER P RIGGS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020340	02/01/2002	MODIFICATION TO HI-TORQUE WHISPER LS AND MS GUIDE WIRES WITH HYDROCOAT HYDROPHILIC COATING	GUIDANT CORP.
K983033	08/31/1998	ACS HT BALANCE MIDDLEWEIGHT GUIDE WIRE	GUIDANT CORP.
K013092	09/17/2001	HI-TOQUE WHISPER LS AND MS GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING	GUIDANT CORP.
K060449	02/21/2006	HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE	GUIDANT CORPORATION
K021228	04/18/2002	HI-TORQUE BALANCE, BALANCE MIDDLEWEIGHT, BALANCE HEAVYWEIGHT, BALANCE TREK AND THE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE	GUIDANT CORP.
K011464	05/14/2001	RX VIATRAC 14 PERIPHERAL DILATATION CATHETER, OTW VIATRAC 18 PERIPHERAL DILATATION CATHETER, RX HERCULINK 14 BILIARY STN	VASCULAR INTERVENTION
K013833	11/19/2001	HI-TOQUE BALANCE MIDDLEWEIGHT UNIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, #1009659,1009659J, 1009660, 10096	GUIDANT CORP.