ClearanceBrief
510(k) K802011 ยท FLN Monitor, Electric For Gravity Flow Infusion Systems

INFUSSION ALARM SYSTEM I.A.S. CAT.#1118

ApplicantPollak (Intl.), Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 31, 1980
ReceivedAug 20, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802011

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.