← HHS Federal Register rules

Medical Devices; Dental Devices; Classification of the Neuromuscular Tongue Muscle Stimulator for the Reduction of Snoring and Obstructive Sleep Apnea

fda-device · Food and Drug Administration · Rule · Published 2024-09-03 · Effective 2024-09-03 · 89 FR 71153

Document

Document number
2024-19725
Federal Register citation
89 FR 71153
CFR reference
21 CFR 872
Type
Rule
Action
Final amendment; final order.
Category
fda-device
Sub-agency
Food and Drug Administration
Publication date
2024-09-03
Effective date
2024-09-03
HHS docket
Docket No. FDA-2024-N-3948

Abstract

The Food and Drug Administration (FDA, Agency, or we) is classifying the neuromuscular tongue muscle stimulator for the reduction of snoring and obstructive sleep apnea into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the neuromuscular tongue muscle stimulator for the reduction of snoring and obstructive sleep apnea's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices.

Source

Authoritative
Federal Register document
Machine
JSON-LD · Markdown