Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062236 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Dimension Vista® CSA and CSAE The Cyclosporine method is an in vitro diagnostic test for the quan... | 2 | 05/21/2014 | Siemens Healthcare Diagnostics, Inc. |
| Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitat... | 2 | 01/23/2014 | Siemens Healthcare Diagnostics, Inc. |
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