ClearanceBrief
510(k) K915496 ยท DQX Wire, Guide, Catheter

DESERET GUIDEWIRE INTRODUCER

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT, US
DecisionSubstantially Equivalent, Feb 27, 1992
ReceivedDec 9, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915496

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.