ClearanceBrief
510(k) K896579 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

GOOSEN URINARY DRAINAGE SYSTEM

ApplicantGoosen Enterprises, Inc., Goldenrod FL, US
DecisionSubstantially Equivalent, Feb 15, 1990
ReceivedNov 20, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K896579

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.