Company ยท US
Cordis Europa, N.V.
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2007. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 16, 2007 | K071189 | CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER Cordis Europa, N.V., NL | LIT |
| Mar 7, 2007 | K063563 | CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER Cordis Europa, N.V. | LIT |
| Apr 11, 2006 | K060302 | INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED Cordis Europa, N.V., NL | KNQ |
| Feb 4, 2005 | K043605 | INSCOPE 3-STAGE BALLOON DILATOR Cordis Europa, N.V., NL | KNQ |
| Jun 21, 2004 | K040413 | CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM Cordis Europa, N.V. | FGE |
| Oct 2, 2003 | K032737 | CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA Cordis Europa, N.V. | DQY |
| Aug 1, 2001 | K012056 | CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM Cordis Europa, N.V. | FGE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||