Medical Device Recalls
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1 result found
510(K) Number: K043244 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Optiflux F18Nre Flux Dialyzers; Product Number: 0500308E. Single Use acute or chronic hemanalysis... | 2 | 02/26/2014 | Fresenius Medical Care Holdings, Inc. |
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