ClearanceBrief
510(k) K190060 ยท EZL Catheter, Retention Type, Balloon

Urethrotech UCD

ApplicantUrethrotech, Kingston Upon Thames, GB
DecisionSubstantially Equivalent, Oct 4, 2019
ReceivedJan 11, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190060

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.