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

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.

510(k) submissions have been managed by Boston Scientific Corporation as regulatory consultant.