ClearanceBrief
510(k) K823204 ยท FRN Pump, Infusion

BETATRON II

ApplicantCardiac Pacemakers, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 30, 1982
ReceivedOct 27, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823204

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.