ClearanceBrief
510(k) K090003 ยท KZE Injector, Fluid, Non-Electrically Powered

ZETAJET

ApplicantBioject, Inc., Tualatin OR, US
DecisionSubstantially Equivalent, Apr 2, 2009
ReceivedJan 2, 2009
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K090003

DateFirm and productCodeLinked 510(k)
May 11, 2012CaridianBCT, Inc.
Trima Accel Automated Blood Collection System, catalog number 917000000, Caridian BCT, Lakewood, CO 80215 USA. Product Usage: Automated Blood Collection System for use in humans.
Terminated
KZENone listed

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