ClearanceBrief
510(k) K760093 ยท GBM Catheter, Urethral

CATHETER, SILICONE FOLEY (BARDEX)

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 23, 1976
ReceivedJun 21, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760093

DateFirm and productCodeLinked 510(k)
Sep 23, 2021C.R. Bard Inc
Catalog A897514, SureStep" Foley Tray, Silicone, Drainage Bag, StatLock" Stabilization Device
Open, Classified
GBMNone listed

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