Kaye Products, Inc.

Kaye Products, Inc. — FDA 510(k) Submissions

Kaye Products, Inc. has submitted 12 FDA 510(k) premarket notifications since 1979, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Chair, Adjustable, Mechanical, Wheelchair, Mechanical, Chair, With Casters, Adaptor, Hygiene, Holder, Infant Position . Use the specialty filter in the sidebar to narrow results.