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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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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
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 1 10/16/2025 Olympus Corporation of the Americas
OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 1 10/16/2025 Olympus Corporation of the Americas
BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P150 1 10/16/2025 Olympus Corporation of the Americas
Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Mo... 2 11/17/2023 Aizu Olympus Co., Ltd.
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