CARESTREAM VUE PACS VERSION 11.4 CARESTREAM VUE MOTION APPLICATION

CARESTREAM VUE PACS VERSION 11.4 CARESTREAM VUE MOTION APPLICATION is an FDA 510(k)-cleared medical device (K132824) manufactured by Carestream Health, 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 February 5, 2014. Regulation: 8.