ClearanceBrief
510(k) K905819 ยท DXT Injector And Syringe, Angiographic

MEDRAD VARIBLE INFUSION INJECTOR

ApplicantMedrad, Inc., Pittsburgh PA, US
DecisionSubstantially Equivalent, Sep 16, 1991
ReceivedDec 31, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K905819

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.