Guidant Corporation, Cardiac Surgery is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Guidant Corporation, Cardiac Surgery - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Guidant Corporation, Cardiac Surgery has 8 FDA 510(k) cleared medical devices. Based in S,Mta Clara, US.
Historical record: 8 cleared submissions from 2002 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Guidant Corporation, Cardiac Surgery Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Guidant Corporation, Cardiac Surgery
8 devices
Cleared
Feb 08, 2008
HEARTSTRING III PROXIMAL SEAL SYSTEM
Cardiovascular
15d
Cleared
Jul 28, 2004
GUIDANT MICROWAVE ABLATION SYSTEM
General & Plastic Surgery
69d
Cleared
Feb 20, 2003
ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400
General & Plastic Surgery
115d
Cleared
Feb 14, 2003
GUIDANT SYNCRUS INTERNAL CARDIOVERSION SYSTEM
Cardiovascular
66d
Cleared
Nov 12, 2002
ESSEX DISSECTION CANNULA, MODEL SXD-1100, ESSEX DISSECTION TIP, MODEL SXD-1200
General & Plastic Surgery
15d
Cleared
Aug 28, 2002
VASOVIEW 6 HARVESTING CANNULA, MODELS VH-2000, VH-2001 & VH-2002
General & Plastic Surgery
13d
Cleared
May 24, 2002
SYNCRUS INTERNAL CARDIOVERSION SYSTEM
Cardiovascular
81d
Cleared
Feb 20, 2002
VASOVIEW 5 HARVESTING CANNULA
Obstetrics & Gynecology
35d