FDA clears CorVascular’s VasoGuard

CorVascular announced today that the FDA granted clearance for its VasoGuard V-Series portfolio of devices.

Minneapolis-based CorVascular plans to immediately begin marketing and selling the devices across the country. The newly cleared suite includes five devices, each with a unique combination of sensors and capabilities for physiologic testing. It features a device, touchscreen computer, mobile cart and a number of accessories approved as a system.

CorVascular developed the devices to test for peripheral arterial disease (PAD) and/or peripheral vascular disease (PVD). They could provide early identification to initiate guideline-directed medical therapy, potentially preventing cardiovascular disease, cerebrovascular disease and limb events such as amputation.

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