K232787
- 510(k) number
- K232787
- Device name
- ScanNav Anatomy Peripheral Nerve Block
- Applicant
- Intelligent Ultrasound Limited GB
- Product code
- QRG — Ultrasound Guided Nerve Block Assist
- Decision date
- 2023-10-06
- Date received
- 2023-09-11
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232787.pdf
Official FDA record: K232787
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.