510(k) K192338 ยท NXC Aligner, Sequential
NEOLab Clear Aligners
| Applicant | New England Ortho Lab, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Mar 12, 2020 |
| Received | Aug 28, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K192338
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.