ClearanceBrief
510(k) K844401 ยท FRN Pump, Infusion

REPRO-MED SYSTEMS INFUSION DEVICE

ApplicantRepro-Med Systems, Inc., Middletown NY, US
DecisionSubstantially Equivalent, Mar 12, 1985
ReceivedNov 13, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K844401

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.