Act Genomics - FDA 510(k) Cleared Devices

Act Genomics has 1 FDA 510(k) cleared medical devices. Based in Taipei, TW.

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

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

510(k) submissions have been managed by K2 Regulatory Consulting, LLC as regulatory consultant.