Cleared Traditional

VIDAS TBI (GFAP, UCH-L1)

K240279 · bioMerieux, Inc. · Immunology

May 2024

Decision

90d

Days

Class 2

Risk

About This 510(k) Submission

K240279 is an FDA 510(k) clearance for the VIDAS TBI (GFAP, UCH-L1), a Brain Trauma Assessment Test (Class II — Special Controls, product code QAT), submitted by bioMerieux, Inc. (Hazelwood, US). The FDA issued a Cleared decision on May 1, 2024, 90 days after receiving the submission on February 1, 2024. This device falls under the Immunology review panel. Regulated under 21 CFR 866.5830.

Submission Details

510(k) Number	K240279 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 01, 2024
Decision Date	May 01, 2024
Days to Decision	90 days
Submission Type	Traditional
Review Panel	Immunology (IM)
Summary	Summary PDF

Device Classification

Product Code	QAT — Brain Trauma Assessment Test
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 866.5830
Definition	Intended For In Vitro Diagnostic Use As An Aid In The Evaluation Of Patients With Suspected Mild Traumatic Brain Injury (tbi) In Conjunction With Other Clinical Information To Assist In Determining The Need For Radiologic (e.g., Ct, Mr) Head Imaging Per Current Standard Of Care