PKB

Autosomal Recessive Carrier Screening Gene Mutation Detection System

Product code
PKB
Device name
Autosomal Recessive Carrier Screening Gene Mutation Detection System
Device class
Class 2
21 CFR
21 CFR 866.5940
Medical specialty
Immunology
Marketing pathway
510(K)
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)

FDA classification definition

Autosomal recessive carrier screening gene mutation detection system is a qualitative in vitro molecular diagnostic system used for genotyping of clinically relevant variants in genomic DNA isolated from human peripheral whole blood or saliva specimens intended for prescription use or over-the-counter use. The device is intended for autosomal recessive disease carrier screening in adults of reproductive age. The device is not intended for copy number variation, cytogenetic, or biochemical testing.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: PKB
Classification and pathway per current FDA publications. Data from openFDA (CC0).