XIDF-AWS801, ANGIO WORKSTATION, V5.31

XIDF-AWS801, ANGIO WORKSTATION, V5.31 is an FDA 510(k)-cleared medical device (K141541) manufactured by Toshibamedical Systems Corporation. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 7, 2014. Regulation: 8.