ClearanceBrief
510(k) K853843 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

IV MATE

ApplicantMedtech Intl., Inc., Apopka FL, US
DecisionSubstantially Equivalent, Jan 9, 1986
ReceivedSep 16, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853843

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.