ClearanceBrief
510(k) K833432 ยท KOD Catheter, Urological

CATHETER INSERTION KIT

ApplicantClinipad Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 28, 1983
ReceivedOct 5, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K833432

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.