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Zdrowie i gospodarka · 29/06/2016

FDA Classifies Electrosurgical Device for Over-the-Counter Aesthetic Use as Class II (Special Controls)

The US Food and Drug Administration (FDA) has classified the electrosurgical device for over-the-counter aesthetic use into Class II, requiring special controls to ensure the device's safety and effectiveness, as part of its efforts to regulate medical devices for aesthetic use.

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