ClearanceBrief
510(k) K180182 ยท EYB Catheter, Ureteral, Gastro-Urology

Dual Lumen Ureteral Access Catheter, Flexi-Tip Dual Lumen Ureteral Access Catheter

ApplicantCook Incorporated, Bloomington IN, US
DecisionSubstantially Equivalent, Sep 14, 2018
ReceivedJan 23, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180182

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.