ClearanceBrief
510(k) K912109 ยท GBO Catheter, Nephrostomy, General & Plastic Surgery

URESIL GENERAL PURPOSE DRAINAGE CATHETER

ApplicantUresil Corp., Skokie IL, US
DecisionSubstantially Equivalent, Aug 12, 1991
ReceivedMay 13, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912109

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.