Medical Device Recalls
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1 result found
510(K) Number: K061818 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL is an in vitro diagn... | 3 | 03/25/2013 |
FEI # 2517506 Siemens Healthcare Diagnostics, Inc. |
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