Clearance Summary
SmartGuard Anti-Snoring Device received FDA 510(k) clearance under submission number K200657, sponsored by Smartguard Rx, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-08-23.
- Submission: K200657
- Applicant / Sponsor: Smartguard Rx, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2021-08-23
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.