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Zdrowie i gospodarka · 31/03/2000

FDA Reclassifies 28 Medical Devices from Class III to Class II

The FDA is reclassifying 28 preamendments devices from Class III to Class II, requiring special controls to ensure safety and effectiveness. The reclassification is based on new information and is part of the agency's ongoing efforts to modernize its regulations.

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