Medical Device Recalls
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1 result found
510(K) Number: K053131 |
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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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| Atellica CH Total Bilirubin_2 assay-In vitro Diagnostic for the determination of total bilirubin S... | 2 | 03/20/2020 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
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