Ricoh Company, Ltd.

Ricoh Company, Ltd. — FDA 510(k) Submissions

Ricoh Company, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Source Localization Software For Electroencephalograph Or Magnetoencephalograph . Use the specialty filter in the sidebar to narrow results.