Medical Device Manufacturer · US , Sunnyvale , CA

Revivant Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Revivant Corp. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 4 cleared submissions from 2001 to 2004. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Revivant Corp. Filter by specialty or product code using the sidebar.

Revivant Corp. is one of 25266 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Revivant Corp.

4 devices

1-4 of 4