K250818
- 510(k) number
- K250818
- Device name
- Nerveblox
- Applicant
- Smart Alfa Teknoloji San. Ve Tic. A.S. TR
- Product code
- QRG — Ultrasound Guided Nerve Block Assist
- Decision date
- 2025-08-15
- Date received
- 2025-03-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K250818.pdf
Official FDA record: K250818
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.