ClearanceBrief
510(k) K232245 ยท FGE Stents, Drains And Dilators For The Biliary Ducts

VedDilator ^TM (3-Stage Balloon Dilation Catheter)

ApplicantJiangsu Vedkang Medical Science and Technology Co., Ltd., Changzhou, CN
DecisionSubstantially Equivalent, Feb 15, 2024
ReceivedJul 28, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232245

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.