ClearanceBrief
510(k) K911869 ยท DQY Catheter, Percutaneous

IVT GUIDING CATHETER

ApplicantIntensive Technology, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 16, 1991
ReceivedApr 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911869

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.