HANDHELD PACEMAKER PROGRAMMER & SOFTWAR

HANDHELD PACEMAKER PROGRAMMER & SOFTWAR is an FDA 510(k)-cleared medical device (K842364) manufactured by Cardiac Pacemakers, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 23, 1984. Regulation: 8.