ClearanceBrief
510(k) K830884 ยท FAD Stent, Ureteral

SURGITEKS PERCUTANEOUS ANTEGRADE ALL -

ApplicantMedical Engineering Corp., Mchenry IL, US
DecisionSubstantially Equivalent, May 9, 1983
ReceivedMar 21, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830884

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.