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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 41 Results
510(K) Number: K023984
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BF-XP60 OES Bronchofiberscope, Model No. BF-XP60 2 09/24/2021 FEI # 2429304
Olympus Corporation of the Americas
BF-3C40 OES Bronchofiberscope, Model No. BF-3C40 2 09/24/2021 FEI # 2429304
Olympus Corporation of the Americas
EVIS EXERA BF-XT160 Bronchofibervideoscope, Model No. BF-XT160 2 09/21/2021 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-XT40 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-XT160 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-XP60 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-XP40 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-P60 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-P40 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-P160 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
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