Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K220587 |
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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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Single Use Distal Cover MAJ-2315 Used with: EVIS EXERA III Duodenovideoscope TJF-Q190V- designed to... | 2 | 02/09/2024 | Olympus Corporation of the Americas |
EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V | 2 | 08/28/2023 | Olympus Corporation of the Americas |
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