The following data is part of a premarket notification filed by Brainlab, Inc. with the FDA for Vectorvision.
Device ID | K962939 |
510k Number | K962939 |
Device Name: | VECTORVISION |
Classification | Neurological Stereotaxic Instrument |
Applicant | BRAINLAB, INC. 600 GLEN CT. Moorestown, NJ 08057 |
Contact | Stefan Vilsmeier |
Correspondent | Stefan Vilsmeier BRAINLAB, INC. 600 GLEN CT. Moorestown, NJ 08057 |
Product Code | HAW |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-29 |
Decision Date | 1997-05-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VECTORVISION 85683064 4341403 Live/Registered |
GUARDION HEALTH SCIENCES, INC. 2012-07-20 |
VECTORVISION 78315306 2951464 Live/Registered |
Vector Security, Inc. 2003-10-17 |
VECTORVISION 78036288 2978101 Dead/Cancelled |
BrainLAB AG 2000-11-22 |
VECTORVISION 76182863 not registered Dead/Abandoned |
CNF Transportation Inc. 2000-12-13 |
VECTORVISION 74124305 1706344 Dead/Cancelled |
VectorVision Corporation 1990-12-17 |
VECTORVISION 73550070 1385086 Live/Registered |
E.F. NETTMANN ASSOCIATES, INC. 1985-07-25 |