ClearanceBrief
510(k) K926357 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass

MEDTRONIC BIO-MEDICUS HANDCRANK MODEL 150

ApplicantMedtronic Bio-Medicus, Inc., Eden Prairie MN, US
DecisionSubstantially Equivalent, Jun 2, 1993
ReceivedDec 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926357

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.