K250482
- 510(k) number
- K250482
- Device name
- Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue
- Applicant
- Fissiontech, LLC NY · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2025-05-08
- Date received
- 2025-02-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K250482.pdf
Official FDA record: K250482
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.