Medical Device Recalls
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1 result found
510(K) Number: K024033 |
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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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EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Olympus video system center, lig... | 2 | 05/31/2016 | Olympus Corporation of the Americas |
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