Medical Device Recalls
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1 result found
510(K) Number: K182747 |
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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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EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro... | 2 | 07/01/2019 | Phadia Ab |
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