Avantec Vascular Corp.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K032436 | DURAMAX .018 BILIARY STENT SYSTEM | FGE | 2004-02-04 | View |
| 510(k) | K030638 | DURAMAX .035 BILIARY STENT SYSTEM, MODELS DML0718-80, DML0718-135, DML0818-80, DML0818-135, DML0918-80, DML0918-135, DML | FGE | 2003-07-09 | View |
| 510(k) | K030062 | ADMIRAL .035 DILATATION CATHETER, MODELS ADL0720-80,ADL0720-135,ADL0820-80, ADL0820-135,ADL0920-80,ADL0920-135,ADL1020-0 | LIT | 2003-04-03 | View |
No matching devices.
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