DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)

DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS) is an FDA 510(k)-cleared medical device (K943929) manufactured by Greenleaf Medical Systems, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on May 14, 1995. Regulation: 8.