ClearanceBrief
510(k) K232934 ยท KRD Device, Vascular, For Promoting Embolization

Sunsphere

ApplicantHangzhou Yangshun Medical Technology Co.,Ltd, Hangzhou, CN
DecisionSubstantially Equivalent, May 30, 2024
ReceivedSep 20, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232934

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.