Cordis Europa, N.V.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071189 | CORDIS AVIATOR PLUS PTA BALLOON DILATATION CATHETER | LIT | 2007-05-16 | View |
| 510(k) | K063563 | CORDIS AMILA PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) BALLOON DILATATION CATHETER | LIT | 2007-03-07 | View |
| 510(k) | K060302 | INSCOPE PRECISION BALLOON DILATOR - WIRE GUIDED | KNQ | 2006-04-11 | View |
| 510(k) | K043605 | INSCOPE 3-STAGE BALLOON DILATOR | KNQ | 2005-02-04 | View |
| 510(k) | K040413 | CORDIS PALMAZ BLUE TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | FGE | 2004-06-21 | View |
| 510(k) | K032737 | CORDIS POWERFLEX EXTREME PTA BALLOON CATHETER, CORDIS POWERFLEX PLUS PTA BALLOON CATHETER, CORDIS POWERFLEX P3 PTA | DQY | 2003-10-02 | View |
| 510(k) | K012056 | CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | FGE | 2001-08-01 | View |
No matching devices.
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