ClearanceBrief
510(k) K832165 ยท KOD Catheter, Urological

IMPROVED SILICATH SILICONE ELASTOMER

ApplicantTravenol Laboratories, S.A., Walker MI, US
DecisionSubstantially Equivalent, Aug 8, 1983
ReceivedJul 5, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832165

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.