Medical Device Manufacturer · US , Sunnyvale , CA

Renovorx, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

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.

FDA 510(k) cleared devices by Renovorx, Inc.

4 devices

1-4 of 4