Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K994267 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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