ScanNav Anatomy Peripheral Nerve Block— 510(k) K232787

Name: FDA 510(k) clearance K232787
Creator: U.S. Food and Drug Administration
Published: 2023-10-06

Substantially Equivalent

Intelligent Ultrasound Limited

FDA 510(k) clearance K232787 for ScanNav Anatomy Peripheral Nerve Block, Substantially Equivalent on 2023-10-06. Applicant: Intelligent Ultrasound Limited. Device class: 2.

Clearance details

Applicant: Intelligent Ultrasound Limited
Product code: Code QRG
Device class: Class 2
Regulation: 21 CFR 868.1980
Advisory panel: Anesthesiology
Date received: 2023-09-11
Decision date: 2023-10-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Cardiff, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code QRG

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K250818 — Nerveblox2025-08-15
DEN220024 — ScanNav Anatomy Peripheral Nerve Block2022-10-18

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