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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K994267
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FDA Recall
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2008 Series Hemodialysis Machines: 2008K with the following product code and description: 190305 20... 2 04/29/2015 FEI # 3001451489
Fresenius Medical Care Holdings, Inc.
2008 Series Hemodialysis Machines: 2008K2 with the following product code and description: 190633 2... 2 04/29/2015 FEI # 3001451489
Fresenius Medical Care Holdings, Inc.
Fresenius 2008K, 2008K2 and 2008 K2@home Hemodialysis Machines, Manufactured by Fresenius USA Inc., ... 2 08/15/2010 FEI # 3001451489
Fresenius Medical Care North America
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