Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080403 |
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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 II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has been designed to be u... | 2 | 09/22/2015 | Olympus America Inc. |
Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This instrument has been... | 2 | 02/04/2016 | Olympus Corporation of the Americas |
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