MDILOG, MODEL MDC-511

MDILOG, MODEL MDC-511 is an FDA 510(k)-cleared medical device (K970344) manufactured by Medtrak Technologies, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 5, 1997. Regulation: 8.