Amicon, Inc.

Amicon, Inc. — FDA 510(k) Submissions

Amicon, Inc. has submitted 20 FDA 510(k) premarket notifications since 1976, of which 20 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dialyzer, High Permeability With Or Without Sealed Dialysate System, Clinical Sample Concentrator, Dialyzer, System, Test, Carcinoembryonic Antigen, Unit, Filter, Membrane . Use the specialty filter in the sidebar to narrow results.