ClearanceBrief
510(k) K893693 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

H.U. I.V. DROP COUNTER

ApplicantLi-Lien Corp., San Jose CA, US
DecisionSubstantially Equivalent, Oct 27, 1989
ReceivedMay 16, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893693

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.