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ELISA RF IgM Test Sytem

ZEUS SCIENTIFIC, INC. · Model 2Z9291M · UDI-DI 00845533000970

Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

The ZEUS ELISA Rheumatoid Factor (RF) IgM Test System is intended for the qualitative and semi-quantitative detection of RF IgM class antibody in human sera. The test is intended to be used as an aid in the diagnosis of rheumatoid arthritis and is for In Vitro diagnostic use.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.