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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K151859
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Product Description
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FDA Recall
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Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The Synapse Cardiovascular i... 2 06/02/2021 Fujifilm Medical Systems U.S.A., Inc.
Synapse CV 6. with AR. A web-based application as the primary user interface for the processing o... 2 02/21/2024 FUJIFILM Healthcare Americas Corporation
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