ClearanceBrief
510(k) K850677 ยท DQX Wire, Guide, Catheter

TELEFLEX GUIDEWIRE

ApplicantTeleflexmedical, Inc., Jeffrey NH, US
DecisionSubstantially Equivalent, Sep 17, 1985
ReceivedFeb 21, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850677

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.