FLEXART V3.1 SOFTWARE

FLEXART V3.1 SOFTWARE is an FDA 510(k)-cleared medical device (K962138) manufactured by Toshiba America Mri, Inc.. 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 22, 1996. Regulation: 8.