K234089
- 510(k) number
- K234089
- Device name
- DNA Appliance
- Applicant
- Vivos Therapeutics KY · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2024-09-16
- Date received
- 2023-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K234089.pdf
Official FDA record: K234089
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.