Neurowave Systems, Inc.

Neurowave Systems, Inc. — FDA 510(k) Submissions

Neurowave Systems, Inc. has submitted 3 FDA 510(k) premarket notifications since 2010, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reduced- Montage Standard Electroencephalograph, Non-normalizing Quantitative Electroencephalograph Software, Index-generating Electroencephalograph Software . Use the specialty filter in the sidebar to narrow results.