K252942
- 510(k) number
- K252942
- Device name
- ShaeferH
- Applicant
- Shaeferh, LLC MA · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2026-04-10
- Date received
- 2025-09-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K252942.pdf
Official FDA record: K252942
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.