Medical Device Recalls
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1 result found
510(K) Number: K843963 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in conjunction with bicarbo... | 2 | 06/15/2021 |
FEI # 2150060 Medivators, Inc. |
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