The following data is part of a premarket notification filed by Memory Md Inc with the FDA for Neurocap.
| Device ID | K172866 |
| 510k Number | K172866 |
| Device Name: | NeuroCap |
| Classification | Electrode, Cutaneous |
| Applicant | Memory MD INC 205 E 42nd Street, 14th Floor New York, NY 10017 |
| Contact | Abdus-salaam Muwwakkil |
| Correspondent | Cassie Lee Guangzhou GLOMED Biological Technology Co., Ltd. Suite 306, Kecheng Mansion, No.121 Science Road Guangzhou Science Park Guangzhou, CN 510006 |
| Product Code | GXY |
| CFR Regulation Number | 882.1320 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-20 |
| Decision Date | 2018-04-27 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NEUROCAP 86799355 5152178 Live/Registered |
Polyganics B.V. 2015-10-26 |
![]() NEUROCAP 86762772 5200773 Live/Registered |
MEMORY MD INC 2015-09-21 |