Medical Device Manufacturer · US , Columbia , SC

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

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Obsidio, Inc. has 1 FDA 510(k) cleared medical devices. Based in Columbia, US.

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

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

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

1 devices

1-1 of 1