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FDA Clears Devon’s Newest Pneumatic Compression Device ArterioFlow 7500

April 14th, 2011 Smit Shah Medicine, Surgery, Vascular Surgery


King of Prussia, PA based Devon Medical Devices has announced FDA 510(k) clearance of its new ArterioFlow 7500 sequential pneumatic compression device. The ArterioFlow 7500 utilizes a set of compression sleeves which cyclically squeeze the patient’s feet and calves. This application of pressure can be used to treat diabetic foot ulcers and peripheral arterial disease by emptying the veins in the lower extremities.
From the product page:
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The ArterioFlow™ Model 7500 device is designed for the treatment of peripheral arterial disease, diabetic foot, intermittent claudication, and other chronic disorders of the lower extremities caused by reduced blood supply or ischemia.
The device applies compression to the foot and calf sequentially through the ArterioFlow™ Garments to empty the veins in the lower extremities. In return, the arterial blood is more easily and readily delivered to the feet and blood-deprived tissues.

Press release: Devon Medical Products Receives FDA 510(k) Clearance for ArterioFlow™ Pump that Treats Diabetic Foot, Peripheral Arterial Disorders…
Product page: ArterioFlow™ 7500 Pneumatic Compression Device for Arterial Insufficiency…

Smit Shah

Smit Shah is a biomedical engineer currently working as a consulting analyst at Accenture. He has a Masters in Engineering Management from Duke University. When not working, he enjoys cooking, concerts, and exploring New York City.

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