Guidant Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Guidant Corporation - FDA 510(k) Cleared Devices
15
Total
12
Cleared
0
Denied
Guidant Corporation has 12 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 12 cleared submissions from 2003 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Guidant Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Guidant Corporation
15 devices
Cleared
May 30, 2006
HI-TORQUE ADVANCE AND ADVANCE LITE GUIDE WIRE
Cardiovascular
98d
Cleared
Apr 12, 2006
OMNILINK .035 BILIARY STENT SYSTEM
Gastroenterology & Urology
120d
Cleared
Mar 06, 2006
RX HERCULINK ELITE BILIARY STENT SYSTEM
Gastroenterology & Urology
87d
Cleared
Mar 03, 2006
ACUITY STEERABLE STYLET ACCESSORY
Cardiovascular
128d
Cleared
Feb 13, 2006
EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.
Cardiovascular
115d
Cleared
Sep 21, 2005
GUIDANT VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM, MODEL VH-3000
General & Plastic Surgery
30d
Cleared
Aug 18, 2005
MODIFICATION TO: RX ACCUNET EMBOLIC PROTECTION SYSTEM
Cardiovascular
9d
Cleared
Aug 16, 2005
RX ACCUNET EMBOLIC PROTECTION SYSTEM
Cardiovascular
7d
Cleared
Aug 20, 2004
GUIDANT VASOVIEW 6 HARVESTING CANNULA, MODEL VH-2000
General & Plastic Surgery
28d
Cleared
Aug 06, 2004
FINISHING WIRE SUPPORTRAK
Cardiovascular
37d
Cleared
Jul 12, 2004
CPI LEAD ADAPTERS, MODELS 6017, 6018 AND 6020
Cardiovascular
28d
Cleared
Mar 03, 2004
RAPIDO CUT-AWAY BLEEDBACK CONTROL VALVE (BBCV), MODEL 7568
Cardiovascular
257d
Cleared
Oct 23, 2003
MODIFICATION TO OMNILINK .035 BILIARY STENT SYSTEM
Gastroenterology & Urology
69d
Cleared
Jul 02, 2003
RAPIDO CUT-A-WAY ROTATING HEMOSTASIS VALVE
Cardiovascular
30d
Cleared
Jun 25, 2003
RAPIDO CUT-AWAY GUIDING CATHETER
Cardiovascular
42d