ClearanceBrief
510(k) K800890 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

LINEBERGER EXTERNAL MALE CATHETER

ApplicantLineberger External Catheter Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 20, 1980
ReceivedApr 18, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800890

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.