Bioteque Corporation

Bioteque Corporation — FDA 510(k) Submissions

Bioteque Corporation has submitted 3 FDA 510(k) premarket notifications since 2020, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stents, Drains And Dilators For The Biliary Ducts . Use the specialty filter in the sidebar to narrow results.