Renovorx, Inc. is one of 16087 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renovorx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RenovoCath, RenovoCath, RenovoCath
4
Total
4
Cleared
0
Denied
Renovorx, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Last cleared in 2021. Active since 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Renovorx, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Experien Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Renovorx, Inc.
4 devices