Cleared Traditional

K093420 - XTAG CYP2D6 KIT V3

K093420 is an FDA 510(k) clearance for XTAG CYP2D6 KIT V3, manufactured by Luminex Molecular Diagnostics, Inc.. The device is a Class 2 Chemistry device with product code NTI cleared through the Traditional 510(k) pathway after a 296-day FDA review.

K093420 · Luminex Molecular Diagnostics, Inc. · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Aug 2010
Decision
296d
Days
Class 2
Risk

K093420 is an FDA 510(k) clearance for the XTAG CYP2D6 KIT V3, MODEL I030C0300 (96 TESTS/KIT), TDAS CYP2D6 SOFTWARE (203.... Classified as Drug Metabolizing Enzyme Genotyping Systems (product code NTI), Class II - Special Controls.

Submitted by Luminex Molecular Diagnostics, Inc. (Toronto, Ontario, CA). The FDA issued a Cleared decision on August 26, 2010 after a review of 296 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.3360 - the FDA in vitro diagnostics and chemistry 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 Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Luminex Molecular Diagnostics, Inc. devices

FDA 510(k) Submission Details - K093420

510(k) Number K093420 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 03, 2009
Decision Date August 26, 2010
Days to Decision 296 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
208d slower than avg
Panel avg: 88d · This submission: 296d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NTI Device Classification - Class 2, Special Controls

Product Code NTI Drug Metabolizing Enzyme Genotyping Systems
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.3360
Definition Intended To Identify The Presence Or Absence Of Human Genotypic Markers Encoding Drug Metaboizing Enzymes Using Dna Originating From Clinical Samples. This Type Of Assay Can Be Used As An Aid Determining Treatment Choice And Individualizing Treatment Dose For Therapeutics That Are Metabolized Primarily By The Specific Enzyme Tested By The System.
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 Chemistry devices follow this clearance model.

Regulatory Peers - NTI Drug Metabolizing Enzyme Genotyping Systems

Devices cleared under the same product code (NTI) and FDA review panel - the closest regulatory comparables to K093420.
xTAG CYP2D6 Kit v3
K170492 · Luminex Molecular Diagnostics, Inc. · Aug 2017
XTAG CYP2C19 KIT V3
K131565 · Luminex Molecular Diagnostics, Inc. · Sep 2013
XTAG CYP2D6 KIT V3 (INCLUDING TDAS CYP2D6 SOFTWARE)
K130189 · Luminex Molecular Diagnostics, Inc. · May 2013
ROCHE AMPLICHIP CYP450 TEST
K043576 · Roche Molecular Systems, Inc. · Jan 2005
AMPLICHIP CYP450 TEST, MODEL 04381866190
DEN040011 · Roche Molecular Systems, Inc. · Dec 2004