Medical Device Recalls
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1 result found
510(K) Number: K042045 |
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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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NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case The NxStage PureF... | 2 | 05/02/2013 | NxStage Medical, Inc. |
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