MARS HOLTER ANALYSIS WORKSTATION

MARS HOLTER ANALYSIS WORKSTATION is an FDA 510(k)-cleared medical device (K132437) manufactured by Ge Medical Systems Information Technologies, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 3, 2013. Regulation: 8.