DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST

DUA-900A IMAGE-INTENSIFIED FLUOROSCOPIC X-RAY SYST is an FDA 510(k)-cleared medical device (K922364) 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 September 3, 1992. Regulation: 8.