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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: K191660
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CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use ... 2 08/24/2020 FEI # 3008203003
Biosense Webster (israel), Ltd.
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