Moss Tubes, Inc.

Moss Tubes, Inc. — FDA 510(k) Submissions

Moss Tubes, Inc. has submitted 5 FDA 510(k) premarket notifications since 1999, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubes, Gastrointestinal (and Accessories), Gastrointestinal Tubes With Enteral Specific Connectors, Tube, Nasogastric . Use the specialty filter in the sidebar to narrow results.