ClearanceBrief
510(k) K033881 ยท DXT Injector And Syringe, Angiographic

MEDRAD STELLANT CT INJECTOR SYSTEM WITH IMAGING SYSTEM INTERFACE MODULE

ApplicantMedrad, Inc., Indianola PA, US
DecisionSubstantially Equivalent, Mar 2, 2004
ReceivedDec 15, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K033881

DateFirm and productCodeLinked 510(k)
Nov 16, 2005Medrad Inc
Stellant CT Injection System. Powered Injector with Syringe. Angiographic Injector and Syringe. Model numbers S, SX, D, and DX
Terminated
DXTNone listed

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