SCHILLER EKG COMBI MSG-IM SCOPE & RECORDER

SCHILLER EKG COMBI MSG-IM SCOPE & RECORDER is an FDA 510(k)-cleared medical device (K852281) manufactured by Armstrong Ind., 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 October 8, 1985. Regulation: 8.