FDA 510(k) Applications for Medical Device Product Code "OCO"
(Mouthguard, Migraine/Tension Headache)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K160477 | LUCO HYBRID OSA APPLIANCE INC. | The Luco Hybrid OSA Appliance | 07/29/2016 |
| K202523 | Moonwalker Innovations Inc | TMJ Relax | 06/24/2021 |
| K010876 | NTI-TSS, INC. | NTI TENSION SUPPRESSION SYSTEM | 06/20/2001 |
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