ClearanceBrief
510(k) K230303 ยท QHA X-Ray Angiographic Imaging Based Coronary Vascular Simulation Software Device

AccuFFRangio Plus

ApplicantArteryFlow Technology Co., Ltd., Hangzhou City, CN
DecisionSubstantially Equivalent, Mar 2, 2023
ReceivedFeb 3, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K230303

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.