Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K010050 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use in the quantitative determination of f... | 2 | 02/21/2023 | Siemens Healthcare Diagnostics, Inc. |
ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic use in the quantitative determinatio... | 2 | 02/21/2023 | Siemens Healthcare Diagnostics, Inc. |
ADVIA Centaur Folate 500 test kit- For in vitro diagnostic use in the quantitative determination of ... | 2 | 02/21/2023 | Siemens Healthcare Diagnostics, Inc. |
ADVIA Centaur® Folate (FOL) | 2 | 05/04/2018 | Siemens Healthcare Diagnostics, Inc. |
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