LVIS Corporation

LVIS Corporation — FDA 510(k) Submissions

LVIS Corporation 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 Automatic Event Detection Software For Full-montage Electroencephalograph, Source Localization Software For Electroencephalograph Or Magnetoencephalograph . Use the specialty filter in the sidebar to narrow results.