ClearanceBrief
510(k) K842798 ยท DQO Catheter, Intravascular, Diagnostic

INTRAOPERATIVE ANGIOSCOPE DELIVERY CATH

ApplicantAmerican Edwards Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Aug 10, 1984
ReceivedJul 17, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842798

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.