ClearanceBrief
510(k) K890039 ยท JOL Catheter And Tip, Suction

KLEEN TEST BASIN SET

ApplicantKleen Test Products, Elkhorn WI, US
DecisionSubstantially Equivalent, Oct 24, 1989
ReceivedJan 10, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K890039

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.