Mec/Surgitek Products
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) | K831446 | SURGITEK NEPHROSTENT KIT | FAD | 1983-06-22 | View |
| 510(k) | K830504 | SURGITEK ULTRA-LO CUFF | BTR | 1983-04-12 | View |
No matching devices.
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