ClearanceBrief
510(k) K202929 ยท QAU Hemostatic Device For Endoscopic Gastrointestinal Use

Nexpowder

ApplicantNextbiomedical Co., Ltd., Incheon, KR
DecisionSubstantially Equivalent, Sep 16, 2022
ReceivedSep 29, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202929

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.