510(k) K193623 ยท EBI Resin, Denture, Relining, Repairing, Rebasing
DIOnavi-Denture
| Applicant | Dio Corporation, Busan, KR |
| Decision | Substantially Equivalent, Oct 22, 2020 |
| Received | Dec 26, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193623
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.