ClearanceBrief
510(k) K823487 ยท FAD Stent, Ureteral

BARD URETERAL STENT

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 27, 1983
ReceivedNov 23, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823487

DateFirm and productCodeLinked 510(k)
Oct 13, 2016C.R. Bard, Inc.
Bard Fluoro-4 Silicone Ureteral Stent, Bard Fluoro-4", Silicone Ureteral Coil Stent; Bard Silicone Uretera l Coil Stent with Figure Four, End, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.
Terminated
FADNone listed

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