Cordis Europa, N.V.
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER (K071189) | Cordis Europa, N.V. | 2007-05-16 |
| CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER (K063563) | Cordis Europa, N.V. | 2007-03-07 |
| INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED (K060302) | Cordis Europa, N.V. | 2006-04-11 |
| INSCOPE 3-STAGE BALLOON DILATOR (K043605) | Cordis Europa, N.V. | 2005-02-04 |
| CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM (K040413) | Cordis Europa, N.V. | 2004-06-21 |
| CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA (K032737) | Cordis Europa, N.V. | 2003-10-02 |
| CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM (K012056) | Cordis Europa, N.V. | 2001-08-01 |
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