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Devices · Intelligent Ultrasound Limited

ScanNav Anatomy Peripheral Nerve Block

510(k)K232787AnesthesiologyQRG

Intelligent Ultrasound Limited is listed for ScanNav Anatomy Peripheral Nerve Block (K232787). The FDA list gives October 6, 2023 as the date of the final decision. The lead panel is Anesthesiology, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code QRG as “Ultrasound Guided Nerve Block Assist”: This device provides real-time interpretation and enhanced visualization of live ultrasound images by highlighting anatomical landmarks in preparation for performing regional anesthesia. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K232787

Official FDA database record

Date of final decision
October 6, 2023
Company on the FDA list
Intelligent Ultrasound Limited
Lead panel
Anesthesiology
Primary product code
QRG
openFDA device name for the code
Ultrasound Guided Nerve Block Assist
Device class
2
Regulation number
868.1980
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

This device provides real-time interpretation and enhanced visualization of live ultrasound images by highlighting anatomical landmarks in preparation for performing regional anesthesia.

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