QAZ · Class II — Moderate Risk (510(k) clearance required) · Medical Genetics · 21 CFR 866.6090
Classification
FDA Product Code
QAZ
Device class
Class II — Moderate Risk (510(k) clearance required)
Regulation
21 CFR 866.6090
Review panel
PA
Medical specialty
Medical Genetics
Submission type
1
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N
Definition
A qualitative in vitro molecular diagnostic system used for the detection of select variants in specified cancer-related genes. The device is intended to be used on genomic DNA isolated from human specimens collected by the user. The results of the test provide users with a genetic health risk assessment for developing certain cancers. The test may not include all variants associated with a predisposition of developing cancer and is not intended to describe a persons overall risk of developing any type of cancer nor to aid in determination of treatment or act as a substitute for recommended cancer screenings or appropriate follow-up. The device is for over-the-counter use.