ClearanceBrief
510(k) K183289 ยท FDI Snare, Flexible

ClearGrasp Snare

ApplicantFinemedix Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Mar 6, 2019
ReceivedNov 26, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K183289

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.