ClearanceBrief
510(k) K813537 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

URIFIX

ApplicantIsramed, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 12, 1982
ReceivedDec 18, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813537

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.