ClearanceBrief
510(k) K131179 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass

CENTRIMAG PRIMARY CONSOLE (2ND GENERATION); MAG MONITOR

ApplicantThoratec Corp, Burlington MA, US
DecisionSubstantially Equivalent, Jul 18, 2013
ReceivedApr 25, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K131179

DateFirm and productCodeLinked 510(k)
Oct 12, 2018Thoratec Switzerland GMBH
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood Pumping System.
Terminated
KFMNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.