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Cardiac Science Corporation
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POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A is an FDA 510(k)-cleared medical device (K091943) manufactured by Cardiac Science Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on September 9, 2009. Regulation: 8.