Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K932955 |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref) | 2 | 12/16/2014 |
FEI # 1219913 Siemens Healthcare Diagnostics, Inc |
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