ClearanceBrief
510(k) K181936 ยท DXT Injector And Syringe, Angiographic

DyeVert PLUS EZ Contrast Reduction System

ApplicantOsprey Medical, Inc., Minnetonka MN, US
DecisionSubstantially Equivalent, Oct 25, 2018
ReceivedJul 19, 2018
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K181936

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.