EPICARDIAL, UNIPOLAR LEAD 4951

EPICARDIAL, UNIPOLAR LEAD 4951 is an FDA 510(k)-cleared medical device (K842065) manufactured by Medtronic Vascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 17, 1985. Regulation: 8.