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FDA 510(k) Applications Submitted by JENNIFER PAE 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.
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