← regulations.gov federal rulemaking dockets

Medical Devices; Anesthesiology Devices; Classification of the Device for Sleep Apnea Testing Based on Mandibular Movement

FDA · Rulemaking · Modified 2026-04-22T12:38:42Z

Docket

Docket ID
FDA-2026-N-3929
Agency
FDA
Type
Rulemaking
Last modified
2026-04-22T12:38:42Z
Object ID
0b000064b9265116

Public engagement

Authoritative
regulations.gov docket page
Comments
Public comment thread
Machine
JSON-LD · Markdown