ULTRAEXTEND USWS-900A V2.1 AND V3.1

ULTRAEXTEND USWS-900A V2.1 AND V3.1 is an FDA 510(k)-cleared medical device (K131822) 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 July 22, 2013. Regulation: 8.