MYOGUIDE SYSTEM MODEL 8008

MYOGUIDE SYSTEM MODEL 8008 is an FDA 510(k)-cleared medical device (K111985) manufactured by Intronix Technologies Corp.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 29, 2011. Regulation: 8.