ClearanceBrief
510(k) K052022 ยท DQX Wire, Guide, Catheter

ASAHI PTCA GUIDE WIRE FIELDER

ApplicantAsahi Intecc Co., Ltd., Newport Beach CA, US
DecisionSubstantially Equivalent, Aug 25, 2005
ReceivedJul 26, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K052022

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.