ClearanceBrief
510(k) K883609 ยท FRN Pump, Infusion

ACCES. PACKAGE FOR USE W/CARDIOGEN-82 GENERATOR

ApplicantSquibb Diagnostics, New Brunswick NJ, US
DecisionSubstantially Equivalent, Apr 14, 1989
ReceivedAug 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883609

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.