ClearanceBrief
510(k) K243061 ยท DYB Introducer, Catheter

SonoStik Guide Wire Introducer

ApplicantSonostik, LLC, Canfield OH, US
DecisionSubstantially Equivalent, Nov 4, 2024
ReceivedSep 27, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K243061

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.