ClearanceBrief
510(k) K243910 ยท MVL Cord, Retraction

Retraxil

ApplicantKulzer, LLC, South Bend IN, US
DecisionSubstantially Equivalent, Sep 24, 2025
ReceivedDec 19, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243910

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.