Cordis Europa, N.V.
Cordis Europa, N.V. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 16, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K071189 | CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER | May 16, 2007 |
| K063563 | CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER | March 7, 2007 |
| K060302 | INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED | April 11, 2006 |
| K043605 | INSCOPE 3-STAGE BALLOON DILATOR | February 4, 2005 |
| K040413 | CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | June 21, 2004 |
| K032737 | CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS PO | October 2, 2003 |
| K012056 | CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | August 1, 2001 |