ImmersiveTouch3 and MicrovisTouch

ImmersiveTouch3 and MicrovisTouch is an FDA 510(k)-cleared medical device (K140860) manufactured by Immersivetouch. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 15, 2014. Regulation: 8.