LivaNova USA, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250937 | Venous Return Cannulae | DWF | 2026-03-11 | View |
| 510(k) | K250283 | RAP Femoral Venous Cannulae | DWF | 2025-07-10 | View |
| 510(k) | K233702 | SMARxT Tubing and Connectors | DWE | 2024-08-08 | View |
No matching devices.