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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K120778
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Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Reso... 2 08/02/2024 GE Medical Systems, LLC
Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Res... 2 08/02/2024 GE Medical Systems, LLC
Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic r... 2 08/02/2017 GE Medical Systems, LLC
GE Healthcare MR superconducting magnets, a component of GE Healthcare Brivo MR355 System, nuclear m... 2 02/09/2022 GE Healthcare, LLC
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