Guidant Corporation, Cardiac Surgery is one of 21874 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
Recent clearances: HEARTSTRING III PROXIMAL SEAL SYSTEM, GUIDANT MICROWAVE ABLATION SYSTEM, ESSEX ASPIRATION/IRRIGATION INSTRUMENT WITH POSITIONING GUIDE, MODEL SY-1400
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.
Regulatory submissions have been managed by N.V. Kema, Kema Quality B.V. and Underwriters Laboratories, Inc..
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