DeviceClearance

Product code QRG— Anesthesiology

ScanNav Anatomy Peripheral Nerve Block

Classification name
Ultrasound Guided Nerve Block Assist
Device class
Class 2
Regulation
21 CFR 868.1980
Advisory panel
Anesthesiology
Total cleared
3
First cleared
Most recent

FDA classification definition

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

— U.S. Food and Drug Administration, device classification record for product code QRG under 21 CFR 868.1980, via openFDA

Market context for product code QRG

FDA has cleared 3 devices under product code QRG between 2022 and 2025, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code QRG

Recent clearances under product code QRG

Data sourced from openFDA. This site is unofficial and independent of the FDA.