Everest & Jennings, Inc.

Everest & Jennings, Inc. — FDA 510(k) Submissions

Everest & Jennings, Inc. has submitted 30 FDA 510(k) premarket notifications since 1983, of which 30 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Wheelchair, Powered, Wheelchair, Mechanical, Vehicle, Motorized 3-wheeled, Generator, Oxygen, Portable . Use the specialty filter in the sidebar to narrow results.