Zdrowie i gospodarka · 06/06/2022
FDA Classifies Non-Implanted Electrical Stimulation Device for Premature Ejaculation into Class II with Special Controls
The FDA is classifying the non-implanted electrical stimulation device for premature ejaculation into Class II with special controls, aiming to ensure safety and effectiveness, and improve patient access to innovative devices.
Source: Federal Register — Food and Drug AdministrationOpen original release →