Cutting Edge Technologies, Inc.
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) | K963595 | SERAGARD VASCULAR ACCESS DEVICE | FMI | 1997-01-06 | View |
| 510(k) | K952606 | TARGETT PATCH | KGX | 1995-12-21 | View |
No matching devices.
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