Edwards Lifesiences, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2022-12-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222117 | Swang-Ganz IQ pulmonary artery catheter | DYG | 2022-12-09 | View |
| 510(k) | K201446 | HemoSphere Advanced Monitoring Platform, HemoSphere ClearSight Module | DQK | 2020-10-01 | View |
No matching devices.