510(k) K212772 ยท NXC Aligner, Sequential
Precision Align
| Applicant | Precision Align, LLC, Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Jan 15, 2022 |
| Received | Aug 31, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212772
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.