ClearanceBrief
510(k) K961121 ยท LNH System, Nuclear Magnetic Resonance Imaging

KINEMATIC KNEE DEVICE/MAGNETOM OPEN SYSTEM

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Jun 19, 1996
ReceivedMar 21, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961121

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.