510(k) K201719
K201719 is an FDA 510(k) premarket notification submitted by The Snore Reliever Company, LLC for the device "Vital Sleep". The FDA issued a decision of Substantially Equivalent on Jan 14, 2021. The device falls under product code LRK (Device, Anti-Snoring), a Class II device regulated under 21 CFR 872.5570. The Snore Reliever Company, LLC has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 14, 2021
- Date Received
- Jun 23, 2020
- Clearance Type
- Abbreviated
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Anti-Snoring
- Device Class
- Class II
- Regulation Number
- 872.5570
- Review Panel
- DE
- Submission Type
- 510(k)