ClearanceBrief
510(k) K900797 ยท DXS Gauge, Pressure, Coronary, Cardiopulmonary Bypass

STOCKERT SHILEY DUAL PRESSURE CONTROL MODULE XR

ApplicantShiley, Inc., Irvine CA, US
DecisionSubstantially Equivalent, May 10, 1990
ReceivedFeb 20, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900797

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.