ClearanceBrief
510(k) K923097 ยท LJE Catheter, Nephrostomy

URESIL NEPHROSTOMY CATHETER

ApplicantUresil Corp., Skokie IL, US
DecisionSubstantially Equivalent, Sep 14, 1992
ReceivedJun 25, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923097

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.