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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: K160552
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EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is ... 1 05/21/2019 FEI # 2015691
Edwards Lifesciences, LLC
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