MODIFIED PACE*AID MODEL 53

MODIFIED PACE*AID MODEL 53 is an FDA 510(k)-cleared medical device (K871971) manufactured by Cardiac Resucitator Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 23, 1987. Regulation: 8.