510(k) K181372 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function
Argos
| Applicant | Retia Medical, LLC, Valhalla NY, US |
| Decision | Substantially Equivalent, Dec 13, 2018 |
| Received | May 23, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181372
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.