Medical Device Recalls
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1 result found
510(K) Number: K112163 |
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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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| Uterine Electromyographic Monitor -Monica IF24 Interface System Product Usage: The Monica IF24 C... | 2 | 03/14/2018 |
FEI # 2126677 GE Healthcare, LLC |
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