ClearanceBrief
510(k) K820565 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

MALE EXTERNAL CATHETER

ApplicantUrocare Products, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 1, 1982
ReceivedMar 2, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820565

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.