ClearanceBrief
510(k) K800306 ยท KOD Catheter, Urological

FOLEY CATHETER

ApplicantAbco Dealers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 28, 1980
ReceivedFeb 12, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800306

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.