ClearanceBrief
510(k) K841386 ยท KOE Dilator, Urethral

KOLLMANN URETHRAL DILATOR

ApplicantImm Enterprises , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, May 9, 1984
ReceivedMar 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841386

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.