ClearanceBrief
510(k) K900994 ยท DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT.

ApplicantDlp, Inc., Grand Rapids MI, US
DecisionSubstantially Equivalent, Aug 15, 1990
ReceivedMar 2, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900994

DateFirm and productCodeLinked 510(k)
Jul 10, 2017Medtronic Perfusion Systems
DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with flexible lines and standard luer sites to facilitate
Terminated
DTLNone listed

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