ClearanceBrief
510(k) K121845 ยท IYE Accelerator, Linear, Medical

SDX SYSTEM

ApplicantDyn'R Sas, Aix En Provence, FR
DecisionSubstantially Equivalent, Oct 19, 2012
ReceivedJun 25, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121845

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.