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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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