Medical Device Manufacturer · US , Lake Forest , CA

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

7 submissions · 7 cleared · Since 2000

Total

Cleared

Denied

Visicu, Inc. has 7 FDA 510(k) cleared medical devices. Based in Lake Forest, US.

Last cleared in 2022. Active since 2000. Primary specialty: Cardiovascular.

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

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

7 devices

1-7 of 7