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Cardiac Science Corporation
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POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS is an FDA 510(k)-cleared medical device (K102496) 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 June 8, 2011. Regulation: 8.
