ClearanceBrief
510(k) K924491 ยท DYB Introducer, Catheter

INTRODUCER, PERCUTANEOUS -- MODIFICATION

ApplicantMedamicus, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Nov 18, 1992
ReceivedAug 20, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924491

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.