ClearanceBrief
510(k) K980751 ยท FRN Pump, Infusion

SABRATEK 4040 INFUSION PUMP

ApplicantSabratek Corp., Niles IL, US
DecisionSubstantially Equivalent, Feb 24, 1999
ReceivedFeb 26, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980751

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.