RESTING EKG ELECTRODE SERIES

RESTING EKG ELECTRODE SERIES is an FDA 510(k)-cleared medical device (K910494) manufactured by Medtronic Andover Medical, 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 April 21, 1991. Regulation: 8.