Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K033225 |
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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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BF-MP160F: EVIS EXERA Bronchofibervideoscope | 2 | 05/06/2022 | Olympus Corporation of the Americas |
BF-XP160F EVIS EXERA Bronchovideoscope, Model No. BF-XP160F | 2 | 09/24/2021 | Olympus Corporation of the Americas |
Bronchovideoscope BF-XP160F | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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