| Device Type ID | 4296 |
| Device Name | Lens, Spectacle, Non-custom (prescription) |
| Regulation Description | Prescription Spectacle Lens. |
| 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 | 886.5844 [🔎] |
| FDA Device Classification | Class 1 Medical Device |
| Product Code | HQG |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |
| Device Type ID | 4296 |
| Device | Lens, Spectacle, Non-custom (prescription) |
| Product Code | HQG |
| FDA Device Classification | Class 1 Medical Device |
| Regulation Description | Prescription Spectacle Lens. |
| CFR Regulation Number | 886.5844 [🔎] |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | Eyemart Express Ltd | II | Dec-16-2014 |
| 2 | Wal Mart Stores, Inc | II | Jun-17-2014 |