Cleared Traditional

K260160 - VITEK REVEAL GN AST Assay and VITEK REV...

K260160 is the FDA 510(k) clearance for VITEK REVEAL GN AST Assay and VITEK REV... by bioMerieux, Inc.. It is a Class 2 Microbiology device (product code SAN) cleared through the Traditional 510(k) pathway after a 169-day FDA review.

K260160 · bioMerieux, Inc. · Microbiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2026
Decision
169d
Days
Class 2
Risk

K260160 is an FDA 510(k) clearance for the VITEK REVEAL GN AST Assay and VITEK REVEAL AST System. Classified as Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples (product code SAN), Class II - Special Controls.

Submitted by bioMerieux, Inc. (Hazelwood, US). The FDA issued a Cleared decision on July 8, 2026 after a review of 169 days - an extended review cycle.

This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.1650 - the FDA microbiology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.

View all bioMerieux, Inc. devices

Submission Details

510(k) Number K260160 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 2026
Decision Date July 08, 2026
Days to Decision 169 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized Yes - Predetermined Change Control Plan authorized FDA has pre-authorized specific future modifications to this device, a pathway common in AI/SaMD devices.
Regulatory Context
Review time vs. panel average
67d slower than avg
Panel avg: 102d · This submission: 169d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. PCCP authorized - AI/SaMD pathway.

Device Classification

Product Code SAN Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.1650
Definition Automated System That Performs Antimicrobial Susceptibility Testing Using Positive Blood Culture Samples
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Microbiology devices follow this clearance model.

Regulatory Peers - SAN Automated Antimicrobial Susceptibility Test System For Positive Blood Culture Samples

Devices cleared under the same product code (SAN) and FDA review panel - the closest regulatory comparables to K260160.
ASTar BC G- Kit
K253573 · Q-Linea AB · Apr 2026
LifeScale Gram Negative Kit (LSGN) with the LifeScale AST system
K251875 · Affinity Biosensors, LLC · Oct 2025
LifeScale Gram Negative Kit (LSGN) with the LifeScale AST system
K241324 · Affinity Biosensors, LLC · Oct 2024
VITEK REVEAL GN AST Assay and VITEK REVEAL AST System
K230675 · Specific Diagnostics, LLC · Jun 2024
ASTar BC G- Kit and ASTar Instrument
K221688 · Q-Linea AB · Apr 2024
LifeScale Gram Negative Kit (LSGN) with the LifeScale AST System
K211815 · Affinity Biosensors · Apr 2024