CORDIS PACEMAKER PROGRAMMERS 255A & 256A

CORDIS PACEMAKER PROGRAMMERS 255A & 256A is an FDA 510(k)-cleared medical device (K810552) manufactured by Cordis Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on March 19, 1981. Regulation: 8.