Personal Genome Diagnostics

FDA Filings

This page includes the latest FDA filings for Personal Genome Diagnostics. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3011805506
• FEI Number: 3011805506
• Name: PERSONAL GENOME DIAGNOSTICS
• Owner & Operator: Personal Genome Diagnostics
• Contact Address: 3600 Boston Street ; Baltimore MD 21224 US
• Official Correspondent:
  • Jennifer Dickey
  • 1-443-6028833-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 3600 Boston Street ; Baltimore, MD 21224 US
• Establishment Type:
  • Manufacture Device in the United States for Export Only
  • Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K192063 Personal Genome Diagnostics	PGDx Elio Tissue Complete	2020-04-24
PFT PERSONAL GENOME DIAGNOSTICS	PGDx elio diversiPhi	2020-02-04

Similar & Related FDA Registered Companies

• PERSONAL GENOME DIAGNOSTICS INC.