ClearanceBrief
510(k) K860841 ยท DQX Wire, Guide, Catheter

GUIDE WIRE INTRODUCER

ApplicantTarget Therapeutics, Los Angeles CA, US
DecisionSubstantially Equivalent, Apr 28, 1986
ReceivedMar 4, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860841

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.