NeuroEEG
Full-montage Standard Electroencephalograph
MemoryMD Inc.
The following data is part of a premarket notification filed by Memorymd Inc. with the FDA for Neuroeeg.
Pre-market Notification Details
| Device ID | K173460 |
| 510k Number | K173460 |
| Device Name: | NeuroEEG |
| Classification | Full-montage Standard Electroencephalograph |
| Applicant | MemoryMD Inc. 205 East 42nd St 14th FL New York, NY 10017 |
| Contact | Abdus-salaam Muwwakkil |
| Correspondent | Abdus-salaam Muwwakkil MemoryMD Inc. 205 East 42nd St 14th FL New York, NY 10017 |
| Product Code | GWQ |
| CFR Regulation Number | 882.1400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-11-07 |
| Decision Date | 2018-02-16 |
| Summary: | summary |
Trademark Results [NeuroEEG]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NEUROEEG 74684707 not registered Dead/Abandoned |
Computational Diagnostics, Inc. 1995-06-05 |
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