Medical Device Recalls
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1 result found
510(K) Number: K212957 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioButton REF BIOST06040 with Software version 3.0.20 The BioButton System is a remote monitoring... | 2 | 08/14/2024 |
FEI # 3016592682 Biointellisense Inc. |
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