ClearanceBrief
510(k) K813624 ยท DQO Catheter, Intravascular, Diagnostic

ADVANCED CATHETER SYSTEMS CORONARY GUID

ApplicantAdvanced Catheter Systems, Walker MI, US
DecisionSubstantially Equivalent, Jan 22, 1982
ReceivedDec 29, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813624

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.