ClearanceBrief
510(k) K150687 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

DripAssist

ApplicantShift Labs, Seattle WA, US
DecisionSubstantially Equivalent, Oct 13, 2015
ReceivedMar 17, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150687

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.