ClearanceBrief
510(k) K880376 ยท GBS Catheter, Ventricular, General & Plastic Surgery

NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP

ApplicantGenesis Industries, Inc., Spring Valley WI, US
DecisionSubstantially Equivalent, Feb 16, 1988
ReceivedJan 27, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880376

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.