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Zdrowie i gospodarka · 15/11/2001

FDA Reclassifies Three Anesthesiology Devices from Class III to Class II

The FDA is reclassifying three anesthesiology devices from Class III to Class II, requiring special controls to ensure their safety and effectiveness, based on new information and amendments to the Federal Food, Drug, and Cosmetic Act.

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