Medical Device Manufacturer · US , Beaverton , OR

Epitope, Inc.

2 submissions · 2 cleared · Since 1997
2
Total
2
Cleared
0
Denied

Epitope, Inc. — FDA 510(k) Submissions

Epitope, Inc. has submitted 2 FDA 510(k) premarket notifications since 1997, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device . Use the specialty filter in the sidebar to narrow results.

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