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Zdrowie i gospodarka · 30/10/2003

FDA Classifies West Nile Virus IgM Capture Elisa Assay as Class II Device

The FDA has classified the West Nile Virus IgM Capture Elisa assay as a Class II device, requiring special controls to ensure its safety and effectiveness, following a petition submitted under the Federal Food, Drug, and Cosmetic Act.

Source: Federal Register — Food and Drug AdministrationOpen original release →