ClearanceBrief
510(k) K940541 ยท LNH System, Nuclear Magnetic Resonance Imaging

MAGNETIC RESONANCE DIAG DEVICE MAGNETOM VISION (MODIF)

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Nov 7, 1994
ReceivedFeb 7, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940541

No recall in the FDA data names this 510(k).

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