ClearanceBrief
510(k) K780831 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

URINARY CATHETERIZATION SYSTEM W/O FOLEY

ApplicantMedical Devices, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 27, 1978
ReceivedMay 22, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780831

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.