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 |