510(k) K183229 ยท NXC Aligner, Sequential
Argen Clear Aligner
| Applicant | Argen Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, Jun 7, 2019 |
| Received | Nov 20, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183229
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.