ClearanceBrief
510(k) K946296 ยท FAD Stent, Ureteral

QUADRA-COIL URETERAL STENT

ApplicantSurgitek, Racine WI, US
DecisionSubstantially Equivalent, Mar 6, 1995
ReceivedDec 27, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K946296

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.