ClearanceBrief
510(k) K882475 ยท LFX Enzyme Linked Immunoabsorbent Assay, Rubella

AMERLITE RUBELLA ANTIBODY ASSAY, LAN.0200/2200

ApplicantAmersham Corp., Arlington Heights IL, US
DecisionSubstantially Equivalent, Oct 6, 1988
ReceivedJun 15, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882475

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.