ClearanceBrief
510(k) K070213 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

PERFORMER CBP SYSTEM

ApplicantRand S.R.L., Minneapolis MN, US
DecisionSubstantially Equivalent, Mar 21, 2007
ReceivedJan 22, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070213

DateFirm and productCodeLinked 510(k)
Jul 23, 2007Medtronic Perfusion Systems
Medtronic Performer CPB-Universal R2100375. Catologue Number R5100052. The Performer CPB System is an electromechanical extracorporeal support device used during cardiopulmonary bypass procedures.
Terminated
DTQNone listed

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