Fred Sammons, Inc.

Fred Sammons, Inc. — FDA 510(k) Submissions

Fred Sammons, Inc. has submitted 278 FDA 510(k) premarket notifications since 1976, of which 278 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Utensil, Eating, Accessories, Wheelchair, Splint, Hand, And Components, Exerciser, Non-measuring, System, Communication, Non-powered . Use the specialty filter in the sidebar to narrow results.