ClearanceBrief
510(k) K052339 ยท DQX Wire, Guide, Catheter

ASAHI PTCA GUIDE WIRE

ApplicantAsahi Intecc Co., Ltd., Newport Beach CA, US
DecisionSubstantially Equivalent, Nov 30, 2005
ReceivedAug 26, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052339

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.