MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODE

MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODE is an FDA 510(k)-cleared medical device (K900169) 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 January 25, 1990. Regulation: 8.