ClearanceBrief
510(k) K263512 ยท EZD Catheter, Straight

Luja female

ApplicantColoplast Corp., Minneapolis MN, US
DecisionSubstantially Equivalent, Oct 28, 2026
ReceivedSep 29, 2026
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K263512

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.