510(k) K121396 ยท NXC Aligner, Sequential
DYNAFLEX
| Applicant | Dyna Flex, St. Ann MO, US |
| Decision | Substantially Equivalent, Aug 14, 2012 |
| Received | May 9, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K121396
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.