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Zdrowie i gospodarka · 14/03/2017

FDA Classifies Vibratory Counter-Stimulation Device as Class II Medical Device with Special Controls

The US Food and Drug Administration (FDA) has classified the vibratory counter-stimulation device into Class II, a category requiring special controls to ensure the device's safety and effectiveness, as mandated by the FDA.

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