Alcyone MEMS Cannula (AMC) System

Alcyone MEMS Cannula (AMC) System is an FDA 510(k)-cleared medical device (K150660) manufactured by Alcyone Lifesciences, Inc.. This device is classified under the Neurology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 15, 2015. Regulation: 8.