510(k) K173107 ยท DXJ Display, Cathode-Ray Tube, Medical
Vios Central Station Monitor Software, Vios Central Server Software
| Applicant | Vios Medical, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Jul 26, 2018 |
| Received | Sep 29, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173107
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.