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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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BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 1 10/16/2025 Olympus Corporation of the Americas
EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Model Numbers BF-1T150, BF-1T60, BF-P150 BF-P60 and EVIS EXERA BR... 1 11/09/2023 Olympus Corporation of the Americas
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