ClearanceBrief
510(k) K260502 ยท EZD Catheter, Straight

Liv Pre-lubricated Intermittent Catheter

ApplicantHR Healthcare, York PA, US
DecisionSubstantially Equivalent, Mar 12, 2026
ReceivedFeb 13, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K260502

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.