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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K970741
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Automated External Defibrillator (non-wearable). Model number 9200, 9200N, 9200DN, 9200RD, 9210N, 9... 2 08/03/2011 FEI # 2112020
Cardiac Science Corporation
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