ClearanceBrief
510(k) K244038 ยท DXT Injector And Syringe, Angiographic

High Pressure Tubing

ApplicantShandong Int Medical Instruments Co., Ltd., Shandong, CN
DecisionSubstantially Equivalent, Sep 5, 2025
ReceivedDec 30, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K244038

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.