ClearanceBrief
510(k) K950739 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass

3M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEM

Applicant3M Health Care, Sarns, Ann Arbor MI, US
DecisionSubstantially Equivalent, Nov 17, 1995
ReceivedFeb 17, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950739

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.