ClearanceBrief
510(k) K123417 ยท LNH System, Nuclear Magnetic Resonance Imaging

BRIVO MR355, OPTIMA MR360

ApplicantGe Hangwei Medical Systems Co., Ltd., Beijing, CN
DecisionSubstantially Equivalent, Jan 17, 2013
ReceivedNov 6, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123417

DateFirm and productCodeLinked 510(k)
Feb 28, 2025GE Healthcare (China) Co., Ltd.
Brivo MR355, NMRI system
Open, Classified
LNHNone listed
Feb 28, 2025GE Healthcare (China) Co., Ltd.
Optima MR360, NMRI system
Open, Classified
LNHNone listed
Aug 2, 2024GE Medical Systems, LLC
Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
Open, Classified
LNHNone listed
Aug 2, 2024GE Medical Systems, LLC
Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Resonance Imaging System
Open, Classified
LNHNone listed
Dec 23, 2021GE Healthcare, LLC
GE Healthcare MR superconducting magnets, a component of GE Healthcare Brivo MR355/Optima MR360 System, nuclear magnetic resonance imaging system.
Open, Classified
LNHNone listed
Aug 2, 2017GE Medical Systems, LLC
Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan tim
Terminated
LNHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.