Brainomix 360 Triage LVO— 510(k) K231837

Substantially Equivalent

Brainomix Limited

FDA 510(k) clearance K231837 for Brainomix 360 Triage LVO, Substantially Equivalent on 2023-09-28. Applicant: Brainomix Limited. Device class: 2.

Clearance details

Applicant: Brainomix Limited
Product code: Code QAS
Device class: Class 2
Regulation: 21 CFR 892.2080
Advisory panel: Radiology
Date received: 2023-06-22
Decision date: 2023-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oxford, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code QAS

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K260729 — Vascular Assist Occlusion Triage (VAOT) (v1.0)2026-06-18
K261317 — BriefCase-Triage2026-05-14
K253163 — EFAI ERSUITE CT APPENDICITIS ASSESSMENT SYSTEM (APPEN-CT-100)2026-04-22
K252421 — JLK-NCCT2026-03-24

More clearances from Brainomix Limited

K260406 — Brainomix 360 Hyperdensity2026-06-12
K251983 — Brainomix 360 Triage Stroke2025-08-26
K242411 — Brainomix 360 e-Lung2025-02-19
K243294 — Brainomix 360 e-ASPECTS2025-02-14
K242123 — Brainomix 360 e-CTA2025-01-06

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