Medical Device Manufacturer · US , Carpinteria , CA

Dako North America, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2009

Total

Cleared

Denied

Dako North America, Inc. has 4 FDA 510(k) cleared medical devices. Based in Carpinteria, US.

Historical record: 4 cleared submissions from 2009 to 2016. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Dako North America, Inc.

4 devices

1-4 of 4