APLIO ARTIDA, V3.2

APLIO ARTIDA, V3.2 is an FDA 510(k)-cleared medical device (K140729) manufactured by Toshiba America Medical Systems, In.C. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 2014. Regulation: 8.