ClearanceBrief
510(k) K895903 ยท DQX Wire, Guide, Catheter

IVT 0.014 GUIDE WIRE

ApplicantIntensive Technology, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jan 4, 1990
ReceivedOct 6, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895903

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.