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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 45 Results
510(K) Number: K023984
 
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BF-1T60 OES Bronchofiberscope, Model No. BF-1T60 2 09/24/2021 Olympus Corporation of the Americas
BF-3C160: EVIS EXERA Bronchovideoscope 2 05/06/2022 Olympus Corporation of the Americas
BF-3C40 OES Bronchofiberscope, Model No. BF-3C40 2 09/24/2021 Olympus Corporation of the Americas
BF-MP60: OES Bronchofiberscope 2 05/06/2022 Olympus Corporation of the Americas
BF-P60 OES Bronchofiberscope, Model No. BF-P60 2 09/24/2021 Olympus Corporation of the Americas
BF-XP60 OES Bronchofiberscope, Model No. BF-XP60 2 09/24/2021 Olympus Corporation of the Americas
BF-XT160 EVIS EXERA Bronchovideoscope, Model No. BF-XT160 2 09/24/2021 Olympus Corporation of the Americas
BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 1 10/16/2025 Olympus Corporation of the Americas
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