510(k) K193404 ยท NHA Abutment, Implant, Dental, Endosseous
UF(II) Bar holder abutment
| Applicant | Dio Corporation, Busan, KR |
| Decision | Substantially Equivalent, May 18, 2020 |
| Received | Dec 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193404
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.