AngioDynamics receives FDA clearance for AlphaVac F1885 System to treat pulmonary embolism.

AngioDynamics receives FDA clearance for AlphaVac F1885 System to treat pulmonary embolism, enhancing its utility in critical medical scenarios. Pulmonary embolism affects 900,000 people in the US annually and has a mortality rate of 3-14% for intermediate-risk patients. The expanded FDA indication broadens the use of the AlphaVac F1885 System, reducing thrombus burden and improving right ventricular function.

April 04, 2024
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