ClearanceBrief
510(k) K910323 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

BEDSIDE FLUID MANAGEMENT SYSTEM 1000 (FMS-1000)

ApplicantUab Research Foundation, Birmingham AL, US
DecisionSubstantially Equivalent, Oct 3, 1991
ReceivedJan 24, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910323

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.