Renovorx Inc

FDA Filings

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

FDA Registration(s)

• Registration Number: 3011279674
• FEI Number: 3011279674
• Name: RENOVORX, INC.
• Owner & Operator: RenovoRx, Inc.
• Contact Address: 4546 El Camino Real Suite 223; Los Altos CA 94022 US
• Official Correspondent:
  • Debra Cogan
  • 1-408-5150820-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 4546 El Camino Real Ste 223 ; Los Altos, CA 94022 US
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
GUDID 00851994005003 Renovorx, Inc.	RenovoCath MMRC120-DB-1111	2021-10-29
PMN K191606 RenovoRx, Inc.	RenovoCath	2019-08-07
PMN K160067 RenovoRx, Inc.	RenovoCath	2017-03-07
PMN K141175 | MJN RENOVORX, INC.	RenovoCath RC120 catheter	2014-11-11
PMN K141175 RENOVORX, INC.	RENOVOCATH RC120	2014-10-24

Related Finance Registrations

CAGE Code	66BA1	RENOVORX, INC. R & D
DUNS	033461994	RENOVORX, INC.
SEC	0001574094	RenovoRx, Inc. of DELAWARE