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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K082720
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Olympus Airway Mobilescope, Models MAF-GM & MAF-TM. 2 08/31/2023 Olympus Corporation of the Americas
Airway Mobilescope MAF-TM 2 09/29/2018 Olympus Corporation of the Americas
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