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Cardiac Science, Inc.
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POWERHEART AED G3 (MODEL 9390E), POWERHEART AED G3 AUTOMATIC (MODEL 9390A) is an FDA 510(k)-cleared medical device (K052161) manufactured by Cardiac Science, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on October 20, 2005. Regulation: 8.