ClearanceBrief
510(k) K820870 ยท FAD Stent, Ureteral

URETERAL STANT SET

ApplicantVan-Tec, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 26, 1982
ReceivedMar 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820870

DateFirm and productCodeLinked 510(k)
May 21, 2009Boston Scientific Corporation
Boston Scientific, Flexima and Percuflex Drainage Catheter Family (Pigtail Style) UPN# DESCRIPTION M0064101260 Percutaneous Combination Stent/Nephrostomy Catheter 8 Fr Singl
Terminated
FADNone listed

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