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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 45 of 45 Results
510(K) Number: K023984
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Product Description
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Bronchofiberscope BF-XP60 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-1T40 2 09/29/2018 Olympus Corporation of the Americas
Bronchofiberscope BF-XT40 2 09/29/2018 Olympus Corporation of the Americas
Bronchovideoscope BF-1T60 2 09/29/2018 Olympus Corporation of the Americas
Bronchovidescope BF-1T240 2 09/29/2018 Olympus Corporation of the Americas
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