Neurent Medical
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2022-10-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222032 | NEUROMARK System | GEI | 2022-10-26 | View |
| 510(k) | K212666 | Neuromark System | GEI | 2021-10-22 | View |
No matching devices.
Related Clinical Trials
NCT05324397Safety and Efficacy Study of the Neurent Medical NEUROMARK™ System in Subjects With Chronic Rhinitis (CLARITY)COMPLETEDNCT05591989Clinical Evaluation of Safety and Efficacy for the NEUROMARK System in Subjects With Chronic Rhinitis (PARAGON)COMPLETEDNCT05937308NEUROMARK Registry StudyACTIVE_NOT_RECRUITING