510(k) K190583 ยท NXC Aligner, Sequential
DynaFlex
| Applicant | Dyna Flex, St. Ann MO, US |
| Decision | Substantially Equivalent, Jun 27, 2019 |
| Received | Mar 6, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190583
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.