FDA 510(k) Applications for Medical Device Product Code: QDJ ()

FDA 510(k) Applications for Medical Device Product Code "QDJ"

FDA 510(k) Number	Applicant	Device Name	Decision Date
K193492	23andMe, Inc.	23andMe Personal Genome Service (PGS) Pharmacogenetic Reports	08/17/2020
K221885	23andMe, Inc.	23andMe Personal Genome Service (PGS) Pharmacogenetic Reports	10/26/2022
DEN180028	23andMe, Inc.	23andMe Personal Genome Service (PGS) Pharmacogenetic Reports	10/31/2018