| Device Type ID | 3814 |
| Device Name | Goniometer, Nonpowered |
| Regulation Description | Nonpowered Goniometer. |
| Regulation Medical Specialty | Orthopedic |
| Review Panel | Neurology |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Neurological And Physical Medicine Devices (DNPMD) Physical Medicine And Rehabilitation Devices Branch (PMDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 888.1520 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | KQW |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 3814 |
| Device | Goniometer, Nonpowered |
| Product Code | KQW |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Nonpowered Goniometer. |
| CFR Regulation Number | 888.1520 [🔎] |
| Device Problems | |
|---|---|
Disconnection | 1 |
| Total Device Problems | 1 |