Cdg Biotech

FDA Filings

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

FDA Registration(s)

• Registration Number: 3013023580
• FEI Number: 3013023580
• Name: CDG BIOTECH
• Owner & Operator: CDG Biotech
• Contact Address: 31332 Via Collinas, Unit 106 ; Westlake Village CA 91362 US
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 31332 Via Colinas Ste 106 ; Westlake Village, CA 91362 US
• Establishment Type:
  • Manufacture Device in the United States for Export Only
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
CDP CDG BIOTECH	CDG Biotech Q-Strip T3	2020-04-04
CDP CDG BIOTECH	CDG Biotech Q-Strip FT3	2020-04-04
JLX CDG BIOTECH	CDG Q-Strip 17-OH Progesterone x 24 Tests	2019-04-03
JKD CDG BIOTECH	CDG Q-Strip C-Peptide x 24 Tests	2019-04-03
CIZ CDG BIOTECH	CDG Q-Strip ANDROSTENEDIONE x 24 Tests	2019-04-03
CFP CDG BIOTECH	CDG Q-Strip Insulin x 24 Tests	2019-04-03
CFL CDG BIOTECH	CDG Q-STRIP HGH (Human Growth Hormone)	2019-04-02
JKC CDG BIOTECH	CDG Q-Strip DHEA, DHEA-S DEHYDROEPIANDROSTERONE (FREE AND SULFATE) x 24 tests	2018-10-27