International Medical Devices Database

Manufacturer Address
RenovoRx, Inc., 4546 El Camino Real Ste 282, Los Altos CA 94022-1068
Manufacturer Parent Company (2017)
RenovoRx, Inc.
Source
USFDA
1 Event
- Recall of Device Recall RenovoCath R120 Catheter

One device in the database

Device Recall RenovoCath R120 Catheter

Model / Serial
Model number: MMRC120-DB-1111; Lot number: B2456974A; Expiry 2016-07. Lot B2457150A - all 72 units were either used or returned prior to initiation of recall.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
US Distribution to the states of : CA and FL.
Product Description
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 delivery of fluids, including diagnostic and/or therapeutic agents, to selected sites in the peripheral vascular system.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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RenovoRx, Inc.

One device in the database

Device Recall RenovoCath R120 Catheter