www.fdanews.com/articles/185797-getinge-wins-510k-clearance-for-pulsioflex-monitoring-system
![ClearanceStamp_Gray.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Gray.gif?t=1576043982&width=430)
Getinge Wins 510(k) Clearance for PulsioFlex Monitoring System
February 27, 2018
Getinge received FDA 510(k) clearance for its PulsioFlex Monitoring System and PiCCO Module.
The diagnostic aid is used to measure and monitor blood pressure and cardiopulmonary, circulatory and organ function variables in patients in intensive care units.
The PiCCO Module is used for hemodynamic management of critically ill patients, providing cardiac output measurements both continuously and intermittently.