Barcoview, Medical Imaging Systems
Kortrijk, BE
Barcoview, Medical Imaging Systems appears in FDA device records in Kortrijk, BE. FDA records list 5 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 5
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 5 510(k) clearances for Barcoview, Medical Imaging Systems between 2007 and 2008. The busiest year on record is 2008, with 3. The most recent is 2008, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 2 |
| 2008 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K081109 | CORONIS 5MP MAMMO SL, MODEL MDMG 6121 | LLZ | Substantially Equivalent | |
| K073007 | CORONIS FUSION 6MP DL, MODEL: MDCC 6130 DL | LLZ | Substantially Equivalent | |
| K072875 | NIO 5MP DISPLAY, MODEL E5620 | LLZ | Substantially Equivalent | |
| K073205 | NIO 5MP, MODEL MDNG-5121 | LLZ | Substantially Equivalent | |
| K070726 | NIO COLOR 3MP AND MDNC 3120 | LLZ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain