K262474
- 510(k) number
- K262474
- Device name
- ND Needle Guidance System
- Applicant
- Accurate Access, LLC AZ · US
- Product code
- ITX — Transducer, Ultrasonic, Diagnostic
- Decision date
- 2026-07-27
- Date received
- 2026-07-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K262474.pdf
Official FDA record: K262474
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.