Personal Genome Diagnostics is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Personal Genome Diagnostics - FDA 510(k) Cleared Devices
Recent clearances: PGDx elio tissue complete
1
Total
1
Cleared
0
Denied
Personal Genome Diagnostics has 1 FDA 510(k) cleared medical devices. Based in Baltimore, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Personal Genome Diagnostics Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Personal Genome Diagnostics
1 devices