Clearance Summary
VITAL SLEEP received FDA 510(k) clearance under submission number K092942, sponsored by The Snore Reliever Company, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2010-01-13.
- Submission: K092942
- Applicant / Sponsor: The Snore Reliever Company, LLC
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2010-01-13
Classification & Regulation
This clearance is catalogued under FDA product code LRK and 21 CFR 872.5570, within the Dental review panel as a Class II device.