K201719 is an FDA 510(k) clearance for the Vital Sleep. This device is classified as a Device, Anti-snoring (Class II - Special Controls, product code LRK).
Submitted by The Snore Reliever Company, LLC (North Bergen, US). The FDA issued a Cleared decision on January 14, 2021, 205 days after receiving the submission on June 23, 2020.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.5570.
| 510(k) Number | K201719 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | June 23, 2020 |
| Decision Date | January 14, 2021 |
| Days to Decision | 205 days |
| Submission Type | Abbreviated |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | LRK - Device, Anti-snoring |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.5570 |