ClearanceBrief
510(k) K232578 ยท DQX Wire, Guide, Catheter

VASSALLO GT 018 G12; VASSALLO GT 018 G30

ApplicantFilmec Co. , Ltd., Hagoya-Shi, JP
DecisionSubstantially Equivalent, Oct 11, 2023
ReceivedAug 25, 2023
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K232578

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.