Kaz, Inc.

Kaz, Inc. — FDA 510(k) Submissions

Kaz, Inc. has submitted 2 FDA 510(k) premarket notifications since 1995, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Continuous Measurement Thermometer, Humidifier, Non-direct Patient Interface (home-use) . Use the specialty filter in the sidebar to narrow results.