ClearanceBrief
510(k) K933908 ยท DXT Injector And Syringe, Angiographic

MEDRAD CT CUSTOM CONVENIENCE KIT

ApplicantMedrad, Inc., Pittsburgh PA, US
DecisionSubstantially Equivalent, Feb 25, 1994
ReceivedAug 11, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933908

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.