Cleared Traditional

K120466 - VERIGENE CYP2C19 NUCLEIC ACID TES (2C19)

K120466 is an FDA 510(k) clearance for VERIGENE CYP2C19 NUCLEIC ACID TES (2C19), manufactured by Nanosphere, Inc.. The device is a Class 2 Toxicology device with product code NTI cleared through the Traditional 510(k) pathway after a 265-day FDA review.

K120466 · Nanosphere, Inc. · Toxicology device
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Nov 2012
Decision
265d
Days
Class 2
Risk

K120466 is an FDA 510(k) clearance for the VERIGENE CYP2C19 NUCLEIC ACID TES (2C19). Classified as Drug Metabolizing Enzyme Genotyping Systems (product code NTI), Class II - Special Controls.

Submitted by Nanosphere, Inc. (Northbrook, US). The FDA issued a Cleared decision on November 6, 2012 after a review of 265 days - an extended review cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3360 - the FDA toxicology 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 Toxicology review framework, consistent with the majority of Class II 510(k) submissions.

View all Nanosphere, Inc. devices

FDA 510(k) Submission Details - K120466

510(k) Number K120466 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 15, 2012
Decision Date November 06, 2012
Days to Decision 265 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
178d slower than avg
Panel avg: 87d · This submission: 265d
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 Toxicology devices follow this clearance model.

Regulatory Peers - NTI Drug Metabolizing Enzyme Genotyping Systems

All 9
Devices cleared under the same product code (NTI) and FDA review panel - the closest regulatory comparables to K120466.
XTAG CYP2C19 KIT V3
K131565 · Luminex Molecular Diagnostics, Inc. · Sep 2013
SPARTAN RX CYP2C19 TEST SYSTEM
K123891 · Spartan Bioscience, Inc. · Aug 2013
XTAG CYP2D6 KIT V3 (INCLUDING TDAS CYP2D6 SOFTWARE)
K130189 · Luminex Molecular Diagnostics, Inc. · May 2013
XTAG CYP2D6 KIT V3, MODEL I030C0300 (96 TESTS/KIT), TDAS CYP2D6 SOFTWARE (2030-0254)
K093420 · Luminex Molecular Diagnostics, Inc. · Aug 2010
INVADER UGT1A1 MOLECULAR ASSAY
K051824 · Third Wave Technologies, Inc. · Aug 2005
ROCHE AMPLICHIP CYP450 TEST
K043576 · Roche Molecular Systems, Inc. · Jan 2005