| Device |
retinoscope, ac-powered |
| Regulation Description |
Retinoscope. |
| Regulation Medical Specialty |
Ophthalmic |
| Review Panel |
Ophthalmic |
| Product Code | HKL |
| Submission Type |
510(k)
|
| Regulation Number |
886.1780
|
| Device Class |
2
|
| Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
| GMP Exempt? |
No
|
| Recognized Consensus Standards
|
Guidance Document
- Retinoscope Guidance; Final
|
|
|
Third Party Review
|
Accredited Persons
|