Pulsion Medical Systems SE
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2020-04-30
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K192169 | PulsioFlex Monitoring System with ProAQT Sensor | DXG | 2020-04-30 | View |
| 510(k) | K171620 | PiCCO Catheter | KRB | 2018-02-21 | View |
| 510(k) | K172259 | PulsioFlex Monitoring System | DXG | 2018-01-18 | View |
No matching devices.