Caire, Inc.

Caire, Inc. — FDA 510(k) Submissions

Caire, Inc. has submitted 7 FDA 510(k) premarket notifications since 1995, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Generator, Oxygen, Portable, Unit, Liquid-oxygen, Portable . Use the specialty filter in the sidebar to narrow results.