Medical Device Recalls
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1 result found
510(K) Number: K151858 |
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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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GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories | 2 | 02/16/2017 | Aesculap Implant Systems LLC |
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