K231138
- 510(k) number
- K231138
- Device name
- Aniti-Snore Mouthguard+
- Applicant
- Oscimed SA CH
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2024-01-16
- Date received
- 2023-04-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K231138.pdf
Official FDA record: K231138
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.