Medical Device Recalls
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1 result found
510(K) Number: K151867 |
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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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STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference ... | 2 | 05/10/2023 | Diagnostica Stago, Inc. |
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