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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 41 Results
510(K) Number: K023984
 
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Bronchofiberscope F-1T160 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-160 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-1T60 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-3C160 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-3C40 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofiberscope BF-40 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchofibercope BF-6C240 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-MP160F 2 09/29/2018 FEI # 2429304
Olympus Corporation of the Americas
Bronchovideoscope BF-MP60 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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