ClearanceBrief
510(k) K221593 ยท EZD Catheter, Straight

Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus

ApplicantConvatec, Inc., Greensboro NC, US
DecisionSubstantially Equivalent, Nov 17, 2022
ReceivedJun 2, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K221593

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.