NPQ · Test, Factor V Leiden Mutations, Genomic Dna Pcr

Hematology · 21 CFR 864.7280 · Class 2

Overview

Product CodeNPQ
Device NameTest, Factor V Leiden Mutations, Genomic Dna Pcr
Regulation21 CFR 864.7280
Device ClassClass 2
Review PanelHematology

Identification

Factor V Leiden mutation detection system is a device that allows the detection and genotyping of a single point mutation of the human Factor V gene, referred to as Factor V Leiden mutation, from DNA isolated from human whole peripheral blood. The system consists of different reagents and instruments which includes polymerase chain reaction (PCR) primers, hybridization matrices, thermal cyclers, imagers, and software packages. The detection system is an aid to diagnosis in the evaluation of patients with suspected thrombophilia.

Classification Rationale

FDA concludes that this device, and substantially equivalent devices of this generic type, should be classified into class II. FDA has determined that the Factor V Leiden Kit can be classified in class II with the establishment of special controls, which provide reasonable assurance of the safety and effectiveness of the device type.

Special Controls

*Classification.* Class II (special controls). The special control is FDA's guidance entitled “Class II Special Controls Guidance Document: Factor V Leiden DNA Mutation Detection Systems.” (See § 864.1(d) for the availability of this guidance document.)

Recent Cleared Devices (6 of 6)

RecordDevice NameApplicantDecision DateDecision
K100980INVADER FACTOR VHologic, Inc.Jun 1, 2011SESE
K093129ILLUMINA VERNCODE GENOTYPING TEST FOR FACOR V AND FACTOR IIIllumina, Inc.Apr 28, 2010SESE
K093974ESENOR FII-FV-MTHFR GENOTYPING TEST, ESENOR FII-FV GENOTYPING TEST, ESENOR FII GENOTYPINGOsmetech Molecular DiagnosticsApr 22, 2010SESE
K082118XPERT HEMOSIL FACTOR II & FACTOR V ASSAYCepheidSep 18, 2009SESE
K060564INFINITI SYSTEMAutoGenomics, Inc.Feb 7, 2007SESE
DEN030005FACTOR V LEIDEN KITRoche Diagnostics Corp.Dec 17, 2003DENG

Top Applicants

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