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Zdrowie i gospodarka · 12/11/2002

FDA Publishes Guidance for Intraoral Devices for Snoring and Obstructive Sleep Apnea

The FDA has released a guidance document outlining recommendations for manufacturers of intraoral devices intended to treat snoring and obstructive sleep apnea, in preparation for a final rule classifying these devices as Class II medical devices.

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