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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K023112
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Product Description
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FDA Recall
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Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse Cardiovascular v4.0.8 Synapse Car... 2 05/14/2015 FEI # 1000513161
Fujifilm Medical Systems U.S.A., Inc.
FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture Archiving and Communicati... 2 05/14/2015 FEI # 1000513161
Fujifilm Medical Systems U.S.A., Inc.
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