Fountain Pharmaceuticals, Inc.

Fountain Pharmaceuticals, Inc. — FDA 510(k) Submissions

Fountain Pharmaceuticals, Inc. has submitted 2 FDA 510(k) premarket notifications since 1990, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Beads, Hydrophilic, For Wound Exudate Absorption, Dressing, Wound, Occlusive . Use the specialty filter in the sidebar to narrow results.