VISART
System, Nuclear Magnetic Resonance Imaging
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
The following data is part of a premarket notification filed by Toshiba America Medical Systems, Inc. with the FDA for Visart.
Pre-market Notification Details
| Device ID | K961092 |
| 510k Number | K961092 |
| Device Name: | VISART |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
| Contact | Javad Seyedzadeh |
| Correspondent | Javad Seyedzadeh TOSHIBA AMERICA MEDICAL SYSTEMS, INC. 2441 MICHELLE DR. P.O. BOX 2068 Tustin, CA 92781 -2068 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-03-19 |
| Decision Date | 1996-06-14 |
| Summary: | summary |
Trademark Results [VISART]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VISART 79002035 3109420 Dead/Cancelled |
SHANGHAI VISART TECHNOLOGIES COMPANY, LIMITED 2003-12-24 |
 VISART 74610092 2188012 Dead/Cancelled |
KABUSHIKI KAISHA TOSHIBA 1994-12-12 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.