www.fdanews.com/articles/189606-fda-oks-hemodynamic-monitoring-device
FDA OK’s Hemodynamic Monitoring Device
December 19, 2018
The FDA has granted 510(k) clearance to Retia Medical’s Argos monitor, a hemodynamic monitor that measures an adult patient’s cardiac output in the operating room and ICUs.
The device uses signal processing and algorithms to create a model of the patient’s circulation, giving physicians information that helps them track oxygen delivery and fluid status in high-risk surgeries.
The Argos monitor can directly connect to a vital-sign monitor to reduce costs and remove the need for disposables.