The following data is part of a premarket notification filed by Barco Nv with the FDA for Coronis 5mp.
Device ID | K111990 |
510k Number | K111990 |
Device Name: | CORONIS 5MP |
Classification | System, Image Processing, Radiological |
Applicant | BARCO NV 35 PRESIDENT KENNEDYPARK Kortrijk, BE 8500 |
Contact | Lieven De Wandel |
Correspondent | Lieven De Wandel BARCO NV 35 PRESIDENT KENNEDYPARK Kortrijk, BE 8500 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-07-13 |
Decision Date | 2011-10-17 |