XERORADIOGRAPHY 125 SYSTEM - MODIFIED

XERORADIOGRAPHY 125 SYSTEM - MODIFIED is an FDA 510(k)-cleared medical device (K761022) manufactured by Xeroradiography. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 23, 1976. Regulation: 8.