X-POSURE SYSTEM VERSION 2 RAD

X-POSURE SYSTEM VERSION 2 RAD is an FDA 510(k)-cleared medical device (K002500) manufactured by Pronosco A/S. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 22, 2000. Regulation: 8.