ClearanceBrief
510(k) K230363 ยท DQY Catheter, Percutaneous

CPS Locator 3D Delivery Catheter

ApplicantCenterPoint Systems, LLC, West Valley City UT, US
DecisionSubstantially Equivalent, Mar 9, 2023
ReceivedFeb 10, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K230363

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.