Clearance Summary
THE SNORE PEACE received FDA 510(k) clearance under submission number K981923, sponsored by The Snore Peace Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1998-08-24.
- Submission: K981923
- Applicant / Sponsor: The Snore Peace Group
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 1998-08-24
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.