ClearanceBrief
510(k) K241028 ยท EZD Catheter, Straight

Luja female (20051); Luja female (20052); Luja female (20054); Luja female (20056)

ApplicantColoplast, Plymouth MN, US
DecisionSubstantially Equivalent, Jul 26, 2024
ReceivedApr 15, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241028

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.