Cleveland Medical Devices, Inc.
KINESIA
SKU K063872UPC GYD
In Stock
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IIFDA 510(k) Cleared (K063872)
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Free shipping on orders over $99 · 30-day returns
Cleveland Medical Devices, Inc.
Free shipping on orders over $99 · 30-day returns
KINESIA is an FDA 510(k)-cleared medical device (K063872) manufactured by Cleveland Medical Devices, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 5, 2007. Regulation: 8.
