Cameo, Inc.

Cameo, Inc. — FDA 510(k) Submissions

Cameo, Inc. has submitted 3 FDA 510(k) premarket notifications since 1992, of which 0 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drape, Surgical, Sampler, Amniotic Fluid (amniocentesis Tray) . Use the specialty filter in the sidebar to narrow results.