QVU — High Throughput Dna Sequencing For Hereditary Cancer Predisposition Assessment Test System. Class II

FDA Device Classification

Classification Details

Product Code
QVU
Device Class
Class II
Regulation Number
866.6095
Submission Type
Review Panel
PA
Medical Specialty
Pathology
Implant
No

Definition

A high throughput DNA sequencing for hereditary cancer predisposition assessment test system is a qualitative in vitro diagnostic (IVD) system intended for analysis of human DNA extracted from human specimens to detect germline mutations in a panel of targeted cancer related genes. It is intended to aid in hereditary cancer predisposition assessment by qualified health care professionals in accordance with professional guidelines. The device is not intended for screening, prenatal testing or as a stand-alone diagnostic test. The device is for prescription use only.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
DEN210011invitae corporationInvitae Common Hereditary Cancers PanelSeptember 29, 2023