Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K151792 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Atelia IM 1300 Analyzer for in vitro diagnostic testing of clinical specimens. | 2 | 05/01/2018 | Siemens Healthcare Diagnostics, Inc. |
Analyzer and Atellica IM 1600 Analyzer system for in vitro diagnostic testing of clinical specimens.... | 2 | 05/01/2018 | Siemens Healthcare Diagnostics, Inc. |
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