Cardeon Corp.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042156 | CARDEON COBRA CATHETER | DWF | 2004-10-06 | View |
| 510(k) | K024058 | MODIFICATION TO CARDEON AEGIS CATHETER | DWF | 2002-12-30 | View |
| 510(k) | K022042 | MODIFICATION TO CARDEON ASCENDING BALLOON CANNULA (ABC) | DWF | 2002-09-03 | View |
| 510(k) | K022174 | MODIFICATION TO CARDEON AEGIS CATHETER | DWF | 2002-07-29 | View |
| 510(k) | K013593 | CARDEON AEGIS CATHETER | DWF | 2002-06-24 | View |
| 510(k) | K001371 | CARDEON ASCENDING BALLOON CANNULA (ABC) | DWF | 2000-07-07 | View |
No matching devices.
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