Mc3, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2023-10-04
| 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.