ClearanceBrief
510(k) K850710 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

TRAVENOL FLO-GARD 500 IV MONITOR

ApplicantTravenol Laboratories, S.A., Deerfield IL, US
DecisionSubstantially Equivalent, Apr 4, 1985
ReceivedFeb 22, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850710

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.