ClearanceBrief
510(k) K073380 ยท DTZ Oxygenator, Cardiopulmonary Bypass

SYNTHESIS PH.I.S.I.O. ADULT MEMBRANE OXYGENATOR WITH INTEGRATED ARETERIAL FILTER AND HARDSHELL VENOUS/CARIOTOMY RESERVOI

ApplicantSorin Group Italia S.R.L., Waltham MA, US
DecisionSubstantially Equivalent, Feb 29, 2008
ReceivedDec 3, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K073380

DateFirm and productCodeLinked 510(k)
Jan 14, 2012Sorin Group USA, Inc.
Synthesis PHisio Oxygenator extracorporeal membrane, Sterile EO, Distributed in U.S. by: Sorin Group USA, Inc, 14401 W. 65th Way, Arvada, CO 80004, manufactured by: Sorin Group Italia, Via Statale 12
Terminated
DTZNone listed

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