Company · US

Renovorx, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2014 to 2021. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (0 in 12 months)

1recalls (0 in 12 months)

1recalls that name a 510(k)

Product codes

Code	Device	Records
MJN	Catheter, Intravascular Occluding, Temporary	5

Decided	510(k)	Device and applicant	Code
Aug 23, 2021	K212324	RenovoCath Renovorx, Inc.	MJN
Aug 7, 2019	K191606	RenovoCath Renovorx, Inc.	MJN
Mar 7, 2017	K160067	RenovoCath Renovorx, Inc.	MJN
Oct 24, 2014	K141175	RENOVOCATH RC120 Renovorx, Inc.	MJN

Date	Firm and product	Code	Linked 510(k)
Dec 31, 2015	RenovoRx, Inc. RenovoCath RC 120; Temporary Intravascular Occluding Catheter Model number: MMRC120-DB-1111; Rx only. Cardiovascular: The RenovoCath RC120 Catheter is intended for the isolation of blood flow and del Terminated	MJN	K141175