EPI-SCOPE OPTION FOR Q SERIES CT SYSTEMS

EPI-SCOPE OPTION FOR Q SERIES CT SYSTEMS is an FDA 510(k)-cleared medical device (K962010) manufactured by Philips Medical Systems (Cleveland), 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 March 20, 1997. Regulation: 8.