ClearanceBrief
510(k) K912380 ยท JAA System, X-Ray, Fluoroscopic, Image-Intensified

LASER BEAM LOCALIZER FOR SIREMOBIL 4

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Jul 19, 1991
ReceivedMay 29, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912380

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.