PACEMAKERS, VITATRONS (SERIES 3000)

PACEMAKERS, VITATRONS (SERIES 3000) is an FDA 510(k)-cleared medical device (K760671) manufactured by Vitatron Medical BV. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on November 11, 1976. Regulation: 8.