Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K151767 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical specimens Siemens Material Number... | 2 | 01/29/2019 | Siemens Healthcare Diagnostics, Inc. |
| Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution is a multi-component system for in... | 2 | 10/18/2018 | Siemens Healthcare Diagnostics, Inc. |
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