ClearanceBrief
510(k) K871021 ยท DQO Catheter, Intravascular, Diagnostic

GUIDING CATHETERS 9F JL4

ApplicantDevices For Vascular Intervention, Inc., Redwood City CA, US
DecisionSubstantially Equivalent, Jun 16, 1987
ReceivedMar 16, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871021

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.