510(k) K173381 ยท DXJ Display, Cathode-Ray Tube, Medical
Nexxis OR
| Applicant | Barco N.V., Kortrijk, BE |
| Decision | Substantially Equivalent, Feb 22, 2018 |
| Received | Oct 30, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K173381
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 20, 2025 | Barco N.V. Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331;
MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311;
MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K Open, Classified |
DXJ | None listed |
| Jul 11, 2024 | Barco N.V. MNA-420 ENC HDMI, Material Number K9303311; cathode ray tube display Completed |
DXJ | None listed |
| Sep 29, 2022 | BARCO NV Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A Open, Classified |
DXJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.