ClearanceBrief
510(k) K093397 ยท DQX Wire, Guide, Catheter

TRAXCESS 14EX GUIDEWIRE AND TRAXCESS DOCKING WIRE

ApplicantMicroVention, Inc., Tistin CA, US
DecisionSubstantially Equivalent, Dec 17, 2009
ReceivedOct 30, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093397

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.