Cordis Europa, N.V. is one of 16135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cordis Europa, N.V. - FDA 510(k) Cleared Devices
Recent clearances: CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER, CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER, INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
7
Total
5
Cleared
0
Denied
Cordis Europa, N.V. has 5 FDA 510(k) cleared medical devices. Based in Warren, US.
Historical record: 5 cleared submissions from 2001 to 2007. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cordis Europa, N.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cordis Europa, N.V.
7 devices
Cleared
May 16, 2007
CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER
Cardiovascular
16d
Cleared
Mar 07, 2007
CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION...
Cardiovascular
99d
Cleared
Apr 11, 2006
INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED
Gastroenterology & Urology
64d
Cleared
Feb 04, 2005
INSCOPE 3-STAGE BALLOON DILATOR
Gastroenterology & Urology
36d
Cleared
Jun 21, 2004
CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM
Gastroenterology & Urology
124d
Cleared
Oct 02, 2003
CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA...
Cardiovascular
28d
Cleared
Aug 01, 2001
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM
Gastroenterology & Urology
30d