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 |