The following data is part of a premarket notification filed by Barcoview with the FDA for Nio 5mp-21 And Mdng-5121 Cb.
Device ID | K062621 |
510k Number | K062621 |
Device Name: | NIO 5MP-21 AND MDNG-5121 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 | 2006-09-05 |
Decision Date | 2007-03-19 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05415334001541 | K062621 | 000 |