ClearanceBrief
510(k) K843478 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

PHARMA-PLAST URIDROP-URIDOME

ApplicantZimmar Consulting , Ltd., Walker MI, US
DecisionSubstantially Equivalent, Dec 5, 1984
ReceivedSep 6, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843478

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.