ADAPTER, LEAD, GENERAL ELECTRIC

ADAPTER, LEAD, GENERAL ELECTRIC is an FDA 510(k)-cleared medical device (K770042) manufactured by Cardiac Pacemakers, 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 January 11, 1977. Regulation: 8.