ClearanceBrief
510(k) K220846 ยท FDI Snare, Flexible

CORE-SNARE

ApplicantIncore Co., Ltd., Daegu, KR
DecisionSubstantially Equivalent, Nov 21, 2022
ReceivedMar 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K220846

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.