Marine Polymer Technologies, Inc.

Marine Polymer Technologies, Inc. — FDA 510(k) Submissions

Marine Polymer Technologies, Inc. has submitted 8 FDA 510(k) premarket notifications since 1997, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Bandage, Liquid, Dressing, Wound, Drug, Clamp, Vascular, Wax, Bone, Tape And Bandage, Adhesive . Use the specialty filter in the sidebar to narrow results.