ClearanceBrief
510(k) K000824 ยท DYB Introducer, Catheter

PERCUTANEOUS INTRODUCER, MODEL 10383-XXX

ApplicantMedamicus, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Apr 13, 2000
ReceivedMar 14, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K000824

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.