ClearanceBrief
510(k) K800610 ยท KOE Dilator, Urethral

URETHRAL SOUND

ApplicantG.D. Searle and Co., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 8, 1980
ReceivedMar 17, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800610

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.