Fujirebio America, Inc.

Fujirebio America, Inc. — FDA 510(k) Submissions

Fujirebio America, Inc. has submitted 2 FDA 510(k) premarket notifications since 1991, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Thyroglobulin, Antigen, Antiserum, Control, Antigens, Ha, Treponema Pallidum . Use the specialty filter in the sidebar to narrow results.