VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM

VSU - VISIONSENSE STEREOSCOPIC VISION SYSTEM is an FDA 510(k)-cleared medical device (K081102) manufactured by Visionsense, Ltd.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 2008. Regulation: 8.