ClearanceBrief
510(k) K103377 ยท DQX Wire, Guide, Catheter

CHARTER GUIDEWIRE MODEL 45-281, 45-282, 45-283

ApplicantBrivant, Ltd., Galway, IE
DecisionSubstantially Equivalent, May 18, 2011
ReceivedNov 17, 2010
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K103377

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.