| Primary Device ID | 00850005944591 |
| NIH Device Record Key | 5f7ed2b0-74a5-412f-91a9-a91cb11cb448 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NeuroStar Advanced Therapy System |
| Version Model Number | 3.X to 3.7 System Upgrade Kit (TouchStar Capable) |
| Catalog Number | 81-37000-200 |
| Company DUNS | 134960348 |
| Company Name | NEURONETICS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| 00850005944591 | 3.X to 3.7 System Upgrade Kit for NeuroStar systems that are TouchStar Capable |
| 00850005944584 | 3.X to 3.7 System Upgrade Kit for NeuroStar systems that are not TouchStar Capable |
| 00850005944577 | 2.X to 3.7 System Upgrade Kit |
| 00850005944522 | NeuroStar Mobile Console Version 3.7, 120V |
| 00850005944430 | NeuroStar Mobile Console, recertified |
| 00850005944423 | NeuroStar Mobile Console, recertified |
| 00850005944621 | NeuroStar Mobile Console 3.8, 120V, US |
| 00850005944812 | NeuroStar Advanced Therapy System, recertified |
| 00850005944836 | NeuroStar Advanced Therapy System, recertified |
| 00850005944829 | NeuroStar Advanced Therapy System, recertified |
| 00850005944874 | NeuroStar Advanced Therapy System, Demo |
| 00850005944867 | NeuroStar Advanced Therapy System, Demo |
| 00850005944850 | NeuroStar Advanced Therapy System, Demo |
| 00850005944843 | NeuroStar Advanced Therapy System, Demo |