Zdrowie i gospodarka · 12/11/2002
FDA Classifies Intraoral Devices for Snoring and Obstructive Sleep Apnea
The FDA has classified intraoral devices for snoring and/or obstructive sleep apnea into Class II, requiring special controls to ensure their safety and effectiveness, following recommendations from the Dental Devices Panel.
Source: Federal Register — Food and Drug AdministrationOpen original release →