MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE

MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE is an FDA 510(k)-cleared medical device (K965068) 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 14, 1997. Regulation: 8.