ClearanceBrief
510(k) K254006 ยท MOF Guide, Wire, Catheter, Neurovasculature

Drivewire 35 Guidewire

ApplicantRapid Medical Ltd., Yokneam, IL
DecisionSubstantially Equivalent, Jul 17, 2026
ReceivedDec 15, 2025
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K254006

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.