ClearanceBrief
510(k) K961008 ยท LHI Set, I.V. Fluid Transfer

AUTOMIX 3+3/AS COMPOUNDER SYSTEM

ApplicantBaxter Healthcare Corp, Round Lake IL, US
DecisionSubstantially Equivalent, Oct 10, 1997
ReceivedMar 12, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961008

DateFirm and productCodeLinked 510(k)
Feb 22, 2011Baxter Healthcare Corp.
AUTOMIX 3+3 Compounder with Accusource Monitoring System, product 2M8287; automated nutrition compounders; Baxter Healthcare Corporation, Clintec Nutrition Division, Deerfield, IL 60015 The Automix Co
Terminated
LHINone listed

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