Cleared Traditional

K083846 - XTAG CYSTIC FIBROSIS 39 KIT V2

K083846 is an FDA 510(k) clearance for XTAG CYSTIC FIBROSIS 39 KIT V2, manufactured by Luminex Molecular Diagnostics, Inc.. The device is a Class 2 Pathology device with product code NUA cleared through the Traditional 510(k) pathway after a 251-day FDA review.

K083846 · Luminex Molecular Diagnostics, Inc. · Pathology device
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Optimized for regulatory review, auditing and printing
Sep 2009
Decision
251d
Days
Class 2
Risk

K083846 is an FDA 510(k) clearance for the XTAG CYSTIC FIBROSIS 39 KIT V2, (CFTR 39 KIT V2), MODEL I027C0231, I027D0266,.... Classified as System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection (product code NUA), Class II - Special Controls.

Submitted by Luminex Molecular Diagnostics, Inc. (Toronto, Ontario, CA). The FDA issued a Cleared decision on September 1, 2009 after a review of 251 days - an extended review cycle.

This device falls under the Pathology FDA review panel, regulated under 21 CFR 866.5900 - the FDA pathology 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 Pathology review framework, consistent with the majority of Class II 510(k) submissions.

View all Luminex Molecular Diagnostics, Inc. devices

FDA 510(k) Submission Details - K083846

510(k) Number K083846 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 24, 2008
Decision Date September 01, 2009
Days to Decision 251 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
174d slower than avg
Panel avg: 77d · This submission: 251d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NUA Device Classification - Class 2, Special Controls

Product Code NUA System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 866.5900
Definition The Cftr Gene Mutation Detection System Is A Device Used To Simultaneously Detect And Identify A Panel Of Mutations And Variants In The Cftr Gene. It Is Intended As An Aid In Confirmatory Diagnostic Testing Of Individuals With Suspected Cystic Fibrosis (cf), Carrier Identification, And Newborn Screening. This Device Is Not Intended For Stand-alone Diagnostic Purposes, Prenatal Diagnostic, Pre-implantation Or Population Screening.
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 Pathology devices follow this clearance model.

Regulatory Peers - NUA System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection

Devices cleared under the same product code (NUA) and FDA review panel - the closest regulatory comparables to K083846.
xTAG Cystic Fibrosis 60 Kit v2, xTAG Data Analysis Software (TDAS) CFTR
K163336 · Luminex Molecular Diagnostics, Inc. · Dec 2016
xTAG Cystic Fibrosis 39 Kit v2
K163347 · Luminex Molecular Diagnostics, Inc. · Dec 2016
XTAG CF60 KIT V2
K083845 · Luminex Molecular Diagnostics, Inc. · Dec 2009