Denver Splint Co.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K940798 | SHIPPERT PRESSURE BANDAGE | KGX | 1994-09-28 | View |
| 510(k) | K940133 | THE EXPANDACELL EAR PACK | LRD | 1994-05-23 | View |
| 510(k) | K935724 | THE EXPANDACELL SINUS PACK | EMX | 1994-05-12 | View |
| 510(k) | K922062 | THE DENVER CAUTERY | GEI | 1993-01-12 | View |
No matching devices.
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