ClearanceBrief
510(k) K181613 ยท LNH System, Nuclear Magnetic Resonance Imaging

MAGNETOM Avanto, MAGNETOM Verio with software syngo MR E11D

ApplicantSiemens Medical Solutions USA, Inc., Malvern PA, US
DecisionSubstantially Equivalent, Nov 6, 2018
ReceivedJun 19, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181613

DateFirm and productCodeLinked 510(k)
Sep 30, 2025Siemens Medical Solutions USA, Inc
MAGNETOM Verio Dot. Model Number: 10684333.
Open, Classified
LNHNone listed
Sep 30, 2025Siemens Medical Solutions USA, Inc
MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
Open, Classified
LNHNone listed

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