ClearanceBrief
510(k) K822536 ยท DXT Injector And Syringe, Angiographic

MARK V

ApplicantMedrad, Inc., Walker MI, US
DecisionSubstantially Equivalent, Sep 28, 1982
ReceivedAug 24, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822536

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.