HEARTSTART 2000 DEFIBRILLATION ELECTRODE

HEARTSTART 2000 DEFIBRILLATION ELECTRODE is an FDA 510(k)-cleared medical device (K885186) manufactured by Laerdal Mfg. 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 February 22, 1989. Regulation: 8.