K252374
- 510(k) number
- K252374
- Device name
- Nylon flexTAP(R)
- Applicant
- Airway Technologies D/B/A Airway Management TX · US
- Product code
- LRK — Device, Anti-Snoring
- Decision date
- 2025-09-11
- Date received
- 2025-07-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252374.pdf
Official FDA record: K252374
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.