Medical Device Manufacturer · DK , Golstrup

Dako Denmark A/S - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017

Total

Cleared

Denied

Dako Denmark A/S has 2 FDA 510(k) cleared medical devices. Based in Golstrup, DK.

Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Dako Denmark A/S Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dako Denmark A/S

2 devices

1-2 of 2