The following data is part of a premarket notification filed by Ricoh Company, Ltd. with the FDA for Ricoh Meg.
Device ID | K210199 |
510k Number | K210199 |
Device Name: | RICOH MEG |
Classification | Source Localization Software For Electroencephalograph Or Magnetoencephalograph |
Applicant | Ricoh Company, Ltd. 2-3, Hokuyodai Kanazawa-shi, JP 920-0177 |
Contact | Satoshi Yuuki |
Correspondent | Satoshi Yuuki Ricoh Company, Ltd. 2-3, Hokuyodai Kanazawa-shi, JP 920-0177 |
Product Code | OLX |
CFR Regulation Number | 882.1400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2021-01-25 |
Decision Date | 2021-07-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RICOH MEG 87626522 not registered Live/Pending |
Ricoh Company, Ltd. 2017-09-28 |