ClearanceBrief
510(k) K935668 ยท DXT Injector And Syringe, Angiographic

MEDRAD SPECTRIS MR INJECTOR

ApplicantMedrad, Inc., Indianola PA, US
DecisionSubstantially Equivalent, Sep 25, 1995
ReceivedNov 26, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K935668

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.