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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: K192206
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Merge Cardio, Model/Catalog Number: Version 12.X, Software Version: 12.1, 12.1.1, 12.2, 12.3, 12.3.1... 2 03/20/2025 Merge Healthcare, Inc.
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