Medical Device Manufacturer · DK , Golstrup

Dako Denmark A/S

2 submissions · 2 cleared · Since 2017
2
Total
2
Cleared
0
Denied

Dako Denmark A/S — FDA 510(k) Submissions

Dako Denmark A/S has submitted 2 FDA 510(k) premarket notifications since 2017, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Immunohistochemistry Assay, Antibody, Progesterone Receptor, Immunohistochemistry Antibody Assay, Estrogen Receptor . Use the specialty filter in the sidebar to narrow results.

2 devices
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