ClearanceBrief
510(k) K760440 ยท KOD Catheter, Urological

CATHETER, NATURAL LATEX URETHRAL

ApplicantAkron Catheter, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 20, 1976
ReceivedAug 16, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760440

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.