ClearanceBrief
510(k) K880895 ยท GBS Catheter, Ventricular, General & Plastic Surgery

URESIL WOUND DRAIN TROCAR

ApplicantUresil Corp., Skokie IL, US
DecisionSubstantially Equivalent, Mar 14, 1988
ReceivedMar 2, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880895

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.