ClearanceBrief
510(k) K071925 ยท LNH System, Nuclear Magnetic Resonance Imaging

MAGNETOM ESSENZA

ApplicantSiemens Medical Solutions USA, Inc., Mavern PA, US
DecisionSubstantially Equivalent, Aug 14, 2007
ReceivedJul 12, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071925

DateFirm and productCodeLinked 510(k)
May 25, 2012Siemens Medical Solutions USA, Inc
Siemens MAGNETOM Essenza, Nuclear Magnetic Resonance Imaging System Product Usage: Nuclear magnetic resonance imaging
Terminated
LNHNone listed

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