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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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Product Description
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Recall
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FDA Recall
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2008T Hemodialysis SYS, with CDX 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
2008T Hemodialysis System without CDX 1 10/06/2023 Fresenius Medical Care Holdings, Inc.
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