ClearanceBrief
510(k) K933014 ยท KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type

LIFESTREAM CENTRIFUGEL PUMP INTERFACE #210PI

ApplicantSt. Jude Medical, Inc., Chelmsford MA, US
DecisionSubstantially Equivalent, Sep 28, 1994
ReceivedJun 21, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933014

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.