ClearanceBrief
510(k) K241330 ยท DXE Catheter, Embolectomy

Fogarty Fortis Arterial Embolectomy Catheter

ApplicantEdwards Lifesciences, Irvine CA, US
DecisionSubstantially Equivalent, Jul 2, 2024
ReceivedMay 10, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K241330

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.