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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: K163001
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FDA Recall
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PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl x Open-Ended Single-Lumen Ven... 2 03/26/2020 FEI # 2020394
Bard Peripheral Vascular Inc
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