Clearance Summary
SILENT SLEEP received FDA 510(k) clearance under submission number K082849, sponsored by Craniofacial Pain Center of Idaho. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-07-16.
- Submission: K082849
- Applicant / Sponsor: Craniofacial Pain Center of Idaho
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.5570
- Decision date: 2009-07-16
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.