IMRX
System, Nuclear Magnetic Resonance Imaging
IMRIS, INC.
The following data is part of a premarket notification filed by Imris, Inc. with the FDA for Imrx.
Pre-market Notification Details
| Device ID | K091166 |
| 510k Number | K091166 |
| Device Name: | IMRX |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | IMRIS, INC. 16809 BRIARDALE ROAD Rockville, MD 20855 |
| Contact | Thomas M Tsakeris |
| Correspondent | Thomas M Tsakeris IMRIS, INC. 16809 BRIARDALE ROAD Rockville, MD 20855 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-04-22 |
| Decision Date | 2009-09-02 |
| Summary: | summary |
Trademark Results [IMRX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 IMRX 77558201 not registered Dead/Abandoned |
Inmediata Health Group Corp. 2008-08-28 |
 IMRX 73499628 not registered Dead/Abandoned |
IMRX CORPORATION 1984-09-17 |
 IMRX 73499300 1369672 Dead/Cancelled |
IMRX CORPORATION 1984-09-14 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.