AUTOPULSE RESUSCITATION SYSTEM MODEL 1000

AUTOPULSE RESUSCITATION SYSTEM MODEL 1000 is an FDA 510(k)-cleared medical device (K112998) manufactured by Zoll Circulation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 2012. Regulation: 8.