SYNECTICS LIBERTY SYS COMPRIS DIGITRAPPER MK II MO

SYNECTICS LIBERTY SYS COMPRIS DIGITRAPPER MK II MO is an FDA 510(k)-cleared medical device (K853648) manufactured by Synectics-Dantec. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 17, 1985. Regulation: 8.