RICOH MEG

Source Localization Software For Electroencephalograph Or Magnetoencephalograph

Ricoh Company, Ltd.

The following data is part of a premarket notification filed by Ricoh Company, Ltd. with the FDA for Ricoh Meg.

Pre-market Notification Details

Device IDK210199
510k NumberK210199
Device Name:RICOH MEG
ClassificationSource Localization Software For Electroencephalograph Or Magnetoencephalograph
Applicant Ricoh Company, Ltd. 2-3, Hokuyodai Kanazawa-shi,  JP 920-0177
ContactSatoshi Yuuki
CorrespondentSatoshi Yuuki
Ricoh Company, Ltd. 2-3, Hokuyodai Kanazawa-shi,  JP 920-0177
Product CodeOLX  
CFR Regulation Number882.1400 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-01-25
Decision Date2021-07-02

Trademark Results [RICOH MEG]

Mark Image

Registration | Serial
Company
Trademark
Application Date
RICOH MEG
RICOH MEG
87626522 not registered Live/Pending
Ricoh Company, Ltd.
2017-09-28

© 2021 FDA.report
This site is not affiliated with or endorsed by the FDA.