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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K162599
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IcePearl" 2.1 CX L 90® Cryoablation Needle 2 12/22/2020 FEI # 3002095335
Boston Scientific Corporation
IceFORCE" 2.1 CX L 90® Cryoablation Needle 2 12/22/2020 FEI # 3002095335
Boston Scientific Corporation
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