MDILOG, MODEL MDC-512

MDILOG, MODEL MDC-512 is an FDA 510(k)-cleared medical device (K990185) 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 March 31, 1999. Regulation: 8.