Medical Device Manufacturer · US , Redwood City , CA

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

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Acuvu, Inc. has 2 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Last cleared in 2021. Active since 2018. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Acuvu, Inc. Filter by specialty or product code using the sidebar.

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

2 devices

1-2 of 2