Cresco TI Systems AB
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042354 | MODIFICATION TO: CRESCO TI IMPLANT CONCEPT | DZE | 2004-09-21 | View |
| 510(k) | K981052 | CRESCO TI IMPLANT CONCEPT | DZE | 2001-12-18 | View |
No matching devices.
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