ClearanceBrief
510(k) K072431 ยท DQX Wire, Guide, Catheter

ASAHI PTCA GUIDE WIRE, X-TREME

ApplicantAsahi Intecc Co., Ltd., Santa Ana CA, US
DecisionSubstantially Equivalent, Sep 26, 2007
ReceivedAug 29, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072431

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.