| Device Type ID | 4196 |
| Device Name | Test, Spectacle Dissociation, Battery-powered (lancaster) |
| Regulation Description | Spectacle Dissociation Test System. |
| Regulation Medical Specialty | Ophthalmic |
| Review Panel | Ophthalmic |
| Premarket Review | Office Of Device Evaluation (ODE) Division Of Ophthalmic And Ear, Nose And Throat Devices (DOED) Diagnostic And Surgical Devices Branch (DSDB) |
| Submission Type | 510(K) Exempt |
| CFR Regulation Number | 886.1910 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | HLO |
| GMP Exempt | Yes |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 4196 |
| Device | Test, Spectacle Dissociation, Battery-powered (lancaster) |
| Product Code | HLO |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Spectacle Dissociation Test System. |
| CFR Regulation Number | 886.1910 [🔎] |