This page includes the latest FDA filings for Nordicneurolab Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3007319065 |
| FEI Number | 3007319065 |
| Name | NordicNeuroLab INC. |
| Owner & Operator | NORDICNEUROLAB AS |
| Contact Address | MOLLENDALSVEIEN 1 -- BERGEN NO-12 Hordaland 5009 NO |
| Registration Status | 1 |
| Initial Importer | Y |
| Registration Expiration | 2020-04-25 |
| Registration Address | 234 W FLORIDA ST STE 205 Milwaukee, WI 53204 US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
NordicNeuroLab INC. [NORDICNEUROLAB AS] | fMRI Hardware System | 2019-12-06 |
| NCAGE Code | 561N7 | NORDICNEUROLAB, INC. |
| CAGE Code | 561N7 | NORDICNEUROLAB, INC. |
| S.A.M. Registration | 561N7 [827981379] | NORDICNEUROLAB, INC. |
| DUNS | 827981379 | NordicNeuroLab, Inc. |