ClearanceBrief
510(k) K020666 ยท FMF Syringe, Piston

DUPLOJECT EASY-PREP SYSTEM 1ML, 2ML, 5ML

ApplicantBaxter Healthcare Corp, Glendale CA, US
DecisionSubstantially Equivalent, Jun 24, 2002
ReceivedMar 1, 2002
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K020666

DateFirm and productCodeLinked 510(k)
Nov 24, 2007Baxter Bioscience
Baxter Duploject Easy Prep, Fibrin Sealant Preparation and Application System ISO; Product Codes: 1500949, 1500950, 1500951, 1501250 & 1501252, Baxter Healthcare Corporation, Deerfield, IL 60015
Terminated
FMFNone listed

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