Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K910423 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Olympus Bronchovideoscope, Models BF-3C40 & BF-N20. | 2 | 08/31/2023 |
FEI # 2429304 Olympus Corporation of the Americas |
| BF-N20 OES Bronchofiberscope, Model No. BF-N20 | 2 | 09/24/2021 |
FEI # 2429304 Olympus Corporation of the Americas |
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