FDA 510(k) Applications for Medical Device Product Code "OCO"
|
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 |