Aurex SA (Pty) , Ltd.
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) | K001482 | AURENORM 75 KF | EJT | 2000-06-23 | View |
| 510(k) | K001481 | PALCERAM 49 | EJT | 2000-06-23 | View |
| 510(k) | K001480 | AURECAST 40 B | EJT | 2000-06-21 | View |
| 510(k) | K001479 | PALCERAM 53 | EJT | 2000-06-21 | View |
| 510(k) | K001477 | AURELUX Y 84 PREMIUM | EJT | 2000-06-20 | View |
| 510(k) | K001478 | AURECAST SUPER INLAY | EJT | 2000-06-20 | View |
No matching devices.
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