| Device Type ID | 3652 |
| Device Name | Pinwheel |
| Regulation Description | Pinwheel. |
| Regulation Medical Specialty | Neurology |
| Review Panel | Neurology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Neurological And Physical Medicine Devices (DNPMD) Neurodiagnostic And Neurosurgical Devices Branch (NDNB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 882.1750 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | GWY |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3652 |
| Device | Pinwheel |
| Product Code | GWY |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Pinwheel. |
| CFR Regulation Number | 882.1750 [🔎] |