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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: K131523
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C2 CryoBalloon Focal Catheter, REF FG-1009. C2 CryoBalloon Ablation System is used as a cryosurgica... 2 06/05/2018 FEI # 3008780134
PENTAX of America Inc
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