Medical Device Recalls
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1 result found
510(K) Number: K111952 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Access Folate WHO Calibrators, Part Number: A98033. The Access Folate Calibrators are intended to... | 2 | 10/10/2012 |
FEI # 2050012 Beckman Coulter Inc. |
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