Cordis Europa, N.V.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K071189CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETERMay 16, 2007
K063563CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETERMarch 7, 2007
K060302INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDEDApril 11, 2006
K043605INSCOPE 3-STAGE BALLOON DILATORFebruary 4, 2005
K040413CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEMJune 21, 2004
K032737CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POOctober 2, 2003
K012056CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEMAugust 1, 2001