ClearanceBrief
510(k) K932271 ยท LNH System, Nuclear Magnetic Resonance Imaging

MAGNETIC RESON DIAG DEVICE MAGNETOM PROJECT 016

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Jan 7, 1994
ReceivedApr 28, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932271

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.