Medical Device Recalls
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1 to 10 of 45 Results
510(K) Number: K023984 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bronchovideoscope BF-160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchofiberscope F-1T160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovidescope BF-1T240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-1T60 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-3C160 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-3C40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchofiberscope BF-40 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchofibercope BF-6C240 | 2 | 09/29/2018 | Olympus Corporation of the Americas |
| Bronchovideoscope BF-MP160F | 2 | 09/29/2018 | Olympus Corporation of the Americas |
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