RECORD AND VERIFY MEVATRON ADAPTER

RECORD AND VERIFY MEVATRON ADAPTER is an FDA 510(k)-cleared medical device (K913674) manufactured by Computerized Medical Systems, 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 November 21, 1991. Regulation: 8.