ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)

ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM) is an FDA 510(k)-cleared medical device (K922550) manufactured by Verimed Holdings, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 9, 1992. Regulation: 8.