Electro-Nucleonics, Inc.

Electro-Nucleonics, Inc. — FDA 510(k) Submissions

Electro-Nucleonics, Inc. has submitted 9 FDA 510(k) premarket notifications since 1988, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antisera, Cf, Herpesvirus Hominis 1,2, Antiserum, Cf, Epstein-barr Virus, Hydrazone Colorimetry, Alt/sgpt, Olive Oil Emulsion (turbidimetric), Lipase, Antiserum, Cf, Cytomegalovirus . Use the specialty filter in the sidebar to narrow results.