K233850
- 510(k) number
- K233850
- Device name
- Difiney Anti Snoring Device
- Applicant
- Fissiontech, LLC NY · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2024-04-18
- Date received
- 2023-12-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233850.pdf
Official FDA record: K233850
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.