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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K150708
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FDA Recall
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Fresenius 2008K Series : Hemodialysis System 2 01/13/2017 Fresenius Medical Care Renal Therapies Group, LLC
Fresenius 2008T Series Hemodialysis System 2 01/13/2017 Fresenius Medical Care Renal Therapies Group, LLC
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