510(k) K191823 ยท NXC Aligner, Sequential
Clear-Aligners
| Applicant | Cdb Corporation, Leland NC, US |
| Decision | Substantially Equivalent, Dec 20, 2019 |
| Received | Jul 8, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191823
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.