Medical Device Recalls
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1 result found
510(K) Number: K122599 |
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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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Siemens ADVIA Centaur® Calibrator U, For in vitro diagnostic use in calibrating the following assay... | 2 | 09/28/2016 | Siemens Healthcare Diagnostics, Inc |
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