Velopex International, Inc.

Velopex International, Inc. — FDA 510(k) Submissions

Velopex International, Inc. has submitted 3 FDA 510(k) premarket notifications since 2003, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Processor, Radiographic-film, Automatic, Airbrush . Use the specialty filter in the sidebar to narrow results.