ClearanceBrief
510(k) K810252 ยท FRN Pump, Infusion

STUMARK INFUSOR

ApplicantStumark Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 17, 1981
ReceivedJan 29, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810252

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.