Cordis Corp. - FDA 510(k) Cleared Devices
315
Total
281
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corp. Gastroenterology & Urology ✕
60 devices
Cleared
Mar 12, 2014
FLEXSTENT BILIARY SELF EXPANDING STENT SYSTEM
Gastroenterology & Urology
337d
Cleared
Feb 06, 2008
SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB,...
Gastroenterology & Urology
505d
Cleared
Apr 27, 2006
PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL...
Gastroenterology & Urology
27d
Cleared
Nov 08, 2004
MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
11d
Cleared
Dec 22, 2003
CORDIS PALMAZ GENESIS TRANSHEPATIC BILLARY STENT ON OPTA PRO .035 DELIVERY...
Gastroenterology & Urology
60d
Cleared
Sep 17, 2003
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
68d
Cleared
Sep 04, 2003
MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
24d
Cleared
Jul 07, 2003
MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
27d
Cleared
Jun 16, 2003
MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
61d
Cleared
Mar 10, 2003
SMART NITINOL STENT ENDOSCOPIC BILIARY SYSTEM
Gastroenterology & Urology
31d
Cleared
Dec 18, 2002
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA...
Gastroenterology & Urology
23d
Cleared
Oct 25, 2002
MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
Gastroenterology & Urology
29d
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