Medical Device Recalls
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31 to 32 of 32 Results
510(K) Number: K051087 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Siemens Healthcare Diagnostics, Inc., Dimension Vista Intelligent Laboratory System with Alpha Pinna... | 2 | 09/15/2010 | Siemens Healthcare Diagnostics, Inc. |
User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension Vista 1500 System with ... | 2 | 01/28/2014 | Siemens Healthcare Diagnostics, Inc. |
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