ClearanceBrief
510(k) K860362 ยท KNX Collector, Urine, (And Accessories) For Indwelling Catheter

SILICATH-AG SILICONE ELASTOMER FOLEY CATHETER

ApplicantTravenol Laboratories, S.A., Deerfield IL, US
DecisionSubstantially Equivalent, Apr 29, 1986
ReceivedJan 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860362

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.