Mc3, 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) | K232767 | Nautilus VF ECMO Oxygenator | BYS | 2023-10-04 | View |
| 510(k) | K203409 | MC3 Crescent Jugular Dual Lumen Catheter | PZS | 2021-05-03 | View |
No matching devices.
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