Pulsion Medical Systems SE
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| 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 |
| 510(k) | K122121 | PULSIOFLEX MONITORING SYSTEM WITH PICCO MODULE | DXG | 2012-08-02 | View |
No matching devices.
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