510(k) K230548 ยท MQC Mouthguard, Prescription
Myoaligner Appliance
| Applicant | Myohealth Technologies, LLC, Portland OR, US |
| Decision | Substantially Equivalent, Feb 2, 2024 |
| Received | Feb 28, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230548
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.