The following data is part of a premarket notification filed by Computational Diagnostics, Inc. with the FDA for Neuronet.
Device ID | K952294 |
510k Number | K952294 |
Device Name: | NEURONET |
Classification | Stimulator, Electrical, Evoked Response |
Applicant | COMPUTATIONAL DIAGNOSTICS, INC. 5001 BAUM BLVD., SUITE 426 Pittsburgh, PA 15213 |
Contact | Sharon Enos |
Correspondent | Sharon Enos COMPUTATIONAL DIAGNOSTICS, INC. 5001 BAUM BLVD., SUITE 426 Pittsburgh, PA 15213 |
Product Code | GWF |
CFR Regulation Number | 882.1870 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-05-16 |
Decision Date | 1996-01-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NEURONET 88904028 not registered Live/Pending |
Neurored LLC 2020-05-06 |
NEURONET 87870054 5611503 Live/Registered |
Computational Diagnostics, Inc. 2018-04-10 |
NEURONET 77389625 3719241 Dead/Cancelled |
Advanced Neuromodulation Systems, Inc. 2008-02-06 |
NEURONET 76123141 not registered Dead/Abandoned |
Advanced Cardiovascular Systems, Inc. 2000-09-05 |
NEURONET 74183733 not registered Dead/Abandoned |
Woosley, Julianne B. 1991-07-10 |
NEURONET 74123074 1700397 Dead/Cancelled |
Computational Diagnostics, Inc. 1990-12-13 |
NEURONET 74051849 1729888 Dead/Cancelled |
National Foundation for Brain Research 1990-04-23 |