Panbio, Inc.

Panbio, Inc. — FDA 510(k) Submissions

Panbio, Inc. has submitted 4 FDA 510(k) premarket notifications since 1991, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antigens, All, Leptospira Spp., Test, Fibrinogen, Prothrombin Fragment 1.2, System, Fibrinogen Determination . Use the specialty filter in the sidebar to narrow results.