ClearanceBrief
510(k) K781422 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

KWIK-FLO URINAL SYSTEM

ApplicantThe Grace Mfg. Co., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 7, 1978
ReceivedAug 17, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781422

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.