ClearanceBrief
510(k) K831750 ยท DXS Gauge, Pressure, Coronary, Cardiopulmonary Bypass

PM-3

ApplicantDelta Medical Industries, Mchenry IL, US
DecisionSubstantially Equivalent, Jul 26, 1983
ReceivedJun 1, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831750

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.