
Revivant Corp.
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AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 is an FDA 510(k)-cleared medical device (K040453) manufactured by Revivant 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 March 10, 2004. Regulation: 8.