CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE is an FDA 510(k)-cleared medical device (K920822) manufactured by Siemens-Pacesetter, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on January 21, 1993. Regulation: 8.