Guidant Cardiac and Vascular Surgery
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) | K003889 | ANCURE SHEATH MODEL # 40315, 40320, 40325 | DYB | 2002-01-24 | View |
| 510(k) | K001694 | GUIDANT RETRIEVER DEVICE | DQY | 2001-05-15 | View |
| 510(k) | K003495 | ANCURE LLIAC BALLOON CATHETER | DQY | 2001-02-07 | View |
| 510(k) | K002676 | ENDOVANCE DUALPASS TEAR-AWAY SHEATH INTRODUCER | DYB | 2000-10-30 | View |
| 510(k) | K970470 | EVT EXPANDABLE SHEATH | DRE | 1997-07-31 | View |
| 510(k) | K970469 | EVT ANGIOSCALE ANGIOGRAPHIC CATHETER | DQO | 1997-05-08 | View |
| 510(k) | K970608 | EVT MARKER BOARD | JAA | 1997-04-21 | View |
No matching devices.
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