MAESTRO(R) MODELS 115, 118, 215 AND 218 PACEMAKERS

MAESTRO(R) MODELS 115, 118, 215 AND 218 PACEMAKERS is an FDA 510(k)-cleared medical device (K880326) manufactured by Cardiac Control Systems, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 10, 1988. Regulation: 8.