ClearanceBrief
510(k) K760259 ยท KOD Catheter, Urological

CATHETER 3-WAY SILICONE FOLEY

ApplicantTravenol Laboratories, S.A., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 23, 1976
ReceivedJul 20, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760259

No recall in the FDA data names this 510(k).

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