Medical Device Recalls
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1 result found
510(K) Number: K040468 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Merge Mammo is a multi-modality, vendor-neutral digital mammography workstation that enables imaging... | 2 | 01/14/2014 |
FEI # 3004526608 GE Healthcare It |
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