ClearanceBrief
510(k) K073082 ยท DQX Wire, Guide, Catheter

CPS COURIER GUIDEWIRE

ApplicantBrivant, Ltd., Galway, IE
DecisionSubstantially Equivalent, Jan 9, 2008
ReceivedNov 1, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K073082

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.