ClearanceBrief
510(k) K222059 ยท EZD Catheter, Straight

SpeediCath Flex Set

ApplicantColoplast, Plymouth MN, US
DecisionSubstantially Equivalent, Sep 21, 2022
ReceivedJul 13, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222059

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.