RenovoCath

Catheter, Intravascular Occluding, Temporary

RenovoRx, Inc.

The following data is part of a premarket notification filed by Renovorx, Inc. with the FDA for Renovocath.

Pre-market Notification Details

Device IDK160067
510k NumberK160067
Device Name:RenovoCath
ClassificationCatheter, Intravascular Occluding, Temporary
Applicant RenovoRx, Inc. 4546 El Camino Real, Suite 282 Los Altos,  CA  94022
ContactKamran Najmabadi
CorrespondentRonald S. Warren
Experien Group, LLC 755 N. Mathilda Avenue Sunnyvale,  CA  94085
Product CodeMJN  
CFR Regulation Number870.4450 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2016-01-13
Decision Date2017-03-07
Summary:summary

Trademark Results [RenovoCath]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RENOVOCATH
RENOVOCATH
85956593 4689326 Live/Registered
Renovorx
2013-06-11

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