| Device Type ID | 4291 |
| Device Name | Photocoagulator And Accessories |
| Regulation Description | Ophthalmic Photocoagulator. |
| 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) |
| CFR Regulation Number | 886.4690 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | HQB |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Expansion Pilot Program |
|
| Device Type ID | 4291 |
| Device | Photocoagulator And Accessories |
| Product Code | HQB |
| FDA Device Classification | Class 2 Medical Device |
| Regulation Description | Ophthalmic Photocoagulator. |
| CFR Regulation Number | 886.4690 [🔎] |
| Device Problems | |
|---|---|
Firing Problem | 2 |
Laser | 2 |
Mechanical Problem | 2 |
Break | 1 |
Device Operational Issue | 1 |
| Total Device Problems | 8 |
| Recalls | |||
|---|---|---|---|
| Manufacturer | Recall Class | Date Posted | |
| 1 | Synergetics Inc | II | Jan-30-2014 |