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