510(k) K220835 ยท NXC Aligner, Sequential
Arkligners
| Applicant | Arklign Laboratories, San Jose CA, US |
| Decision | Substantially Equivalent, Aug 12, 2022 |
| Received | Mar 22, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220835
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.