Neurofield, Inc.

Neurofield, Inc. — FDA 510(k) Submissions

Neurofield, Inc. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Full-montage Standard Electroencephalograph, Normalizing Quantitative Electroencephalograph Software, Cranial Electrotherapy Stimulator To Treat Insomnia And/or Anxiety . Use the specialty filter in the sidebar to narrow results.