Cordis Corp.
FDA 510(k) & PMA Approved Devices — 314 products
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Total Devices314
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K112797 | POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER | LIT | 2012-05-04 | View |
| 510(k) | K101651 | ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE, ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE | NTE | 2010-07-09 | View |
| 510(k) | K082143 | MICRO GUIDE CATHETER XP | PDU | 2008-08-25 | View |
| 510(k) | K062798 | SMART NITINOL SELF-EXPANDING STENT, MODEL C06120MB, C07120MB, C08120MB, C06150MB, C07150MB, C08150MB | FGE | 2008-02-06 | View |
| 510(k) | K060877 | PALMAZ BLUE .014 TRANSHEPATIC BILIARY STENT SYSTEM-MODEL PB1550,BAS,BAX,PB1560,BAS,BAX,PB1850,BAS,BAXPB1860BAS,BAX | FGE | 2006-04-27 | View |
| 510(k) | K050645 | CORDIS AMIIA .014 PTA BALLOON CATHETER | LIT | 2005-04-01 | View |
| 510(k) | K040592 | CORDIS STEER-IT DEFLECTING TIP GUIDEWIRE | DQX | 2004-12-17 | View |
| 510(k) | K042969 | MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2004-11-08 | View |
| 510(k) | K033394 | CORDIS PALMAZ GENESIS TRANSHEPATIC BILLARY STENT ON OPTA PRO .035 DELIVERY SYSTEM | FGE | 2003-12-22 | View |
| 510(k) | K032137 | PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2003-09-17 | View |
| 510(k) | K032457 | MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2003-09-04 | View |
| 510(k) | K031777 | MODEIFICATION TO: SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2003-07-07 | View |
| 510(k) | K031197 | MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2003-06-16 | View |
| 510(k) | K030409 | SMART NITINOL STENT ENDOSCOPIC BILIARY SYSTEM | FGE | 2003-03-10 | View |
| 510(k) | K023907 | CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER | KNQ | 2002-12-18 | View |
| 510(k) | K023217 | MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2002-10-25 | View |
| 510(k) | K023116 | CORDIS OPTEASE PERMANENT VENA CAVA FILTER, MODELS 466-F200A, 466-F200B | DTK | 2002-10-18 | View |
| 510(k) | K021898 | SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM | FGE | 2002-08-14 | View |
| 510(k) | K021345 | MODIFICATION TO CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT ON SLALOM .018 DELIVERY SYSTEM | FGE | 2002-06-28 | View |
| 510(k) | K021593 | MODIFICATION TO ENVOY AND VISTA BRITE TIP | DQY | 2002-06-13 | View |
No matching devices.
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