K243752
- 510(k) number
- K243752
- Device name
- Double Tube Herbst Appliance
- Applicant
- The Tmj Clinic PC OR · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2025-09-17
- Date received
- 2024-12-05
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K243752.pdf
Official FDA record: K243752
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.