Medical Device Recalls
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1 result found
510(K) Number: K120418 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HF Cable WA00014A, Endoscopic electrosurgical unit and accessories | 2 | 12/14/2016 | Olympus Corporation of the Americas |
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