Biomagnetic Technologies, Inc.

Biomagnetic Technologies, Inc. — FDA 510(k) Submissions

Biomagnetic Technologies, Inc. has submitted 8 FDA 510(k) premarket notifications since 1979, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Source Localization Software For Electroencephalograph Or Magnetoencephalograph, Magnetoencephalograph, Stimulator, Mechanical, Evoked Response, Ventilator, Continuous, Facility Use . Use the specialty filter in the sidebar to narrow results.