ClearanceBrief
510(k) K982326 ยท MSD Catheter, Hemodialysis, Implanted

MEDI-TECH DIALYSIS CATHETER GASTROENTEROLOGY

ApplicantBoston Scientific Corp, Natick, MA, US
DecisionSubstantially Equivalent, Jul 12, 1999
ReceivedJul 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982326

DateFirm and productCodeLinked 510(k)
Sep 2, 2005Boston Scientific Corporation
Vaxcel Chronic Dialysis Catheter - Catheter/PU/14/23/Plastic Catalog Number : 45-520
Terminated
KOBNone listed

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