Medical Device Recalls
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1 result found
510(K) Number: K080919 |
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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 SL SAK-303 - 2 dialysate sacks (SAK) with concentrate for use with PureFlow SL, Rx ... | 3 | 01/20/2012 | NxStage Medical, Inc. |
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