FDA 510(k) Applications Submitted by BEVERLY MAGRANE

FDA 510(k) Number Submission Date Device Name Applicant
K091943 06/30/2009 POWERHEART AED G3, MODEL 9390E, POWERHEART AED G3 AUTOMATIC, MODEL 9390A CARDIAC SCIENCE CORPORATION
K082090 07/24/2008 9131 DEFIBRILLATION ELECTRODES CARDIAC SCIENCE CORPORATION
K082173 08/01/2008 Q-STRESS AND HEARTSTRIDE, MODELS QSTRESS/Q40 AND H4/H4S CARDIAC SCIENCE CORPORATION


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