ClearanceBrief
510(k) K904959 ยท DQO Catheter, Intravascular, Diagnostic

PSG HEMOSTATIC CONTROL VALVE

ApplicantPeripheral Systems Group, Mountain View CA, US
DecisionSubstantially Equivalent, Dec 17, 1990
ReceivedNov 5, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904959

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.