ClearanceBrief
510(k) K083713 ยท DQX Wire, Guide, Catheter

.035 LOC GUIDE WIRE EXTENSION

ApplicantAbbott Vascular, Santa Clara CA, US
DecisionSubstantially Equivalent, Feb 23, 2009
ReceivedDec 15, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083713

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.