The following data is part of a premarket notification filed by Barcoview with the FDA for Coronis 3mp And Mdcg 3120-cb.
Device ID | K061924 |
510k Number | K061924 |
Device Name: | CORONIS 3MP AND MDCG 3120-CB |
Classification | System, Image Processing, Radiological |
Applicant | BARCOVIEW 35 PRESIDENT KENNEDYPARK Kortrijk, BE B-8500 |
Contact | Lieven De Wandel |
Correspondent | Lieven De Wandel BARCOVIEW 35 PRESIDENT KENNEDYPARK Kortrijk, BE B-8500 |
Product Code | LLZ |
CFR Regulation Number | 892.2050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-07-07 |
Decision Date | 2006-09-05 |
Summary: | summary |