Zdrowie i gospodarka · 03/07/2014
FDA Classifies Nonpowered Lower Extremity Pressure Wrap as Class I Device
The FDA has classified the nonpowered lower extremity pressure wrap as a Class I device, which provides a reasonable assurance of safety and effectiveness, following a classification process to ensure the device meets safety and effectiveness standards.
Source: Federal Register — Food and Drug AdministrationOpen original release →