HOQ — Grid, Amsler Class I
FDA Device Classification
Classification Details
- Product Code
- HOQ
- Device Class
- Class I
- Regulation Number
- 886.1330
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K180895 | oculocare medical | Alleye | June 27, 2018 |
| K143211 | vital art and science incorporated | myVision Track Model 005 | March 20, 2015 |
| K121738 | vital art and science incorporated | MYVISIONTRACK(TM) | February 22, 2013 |
| K014044 | notal vision | MASCULAR COMPUTERIZED PSYCHOPHYSICAL TEST (MCPT) | March 4, 2002 |
| K874252 | richmond products | KREDA DISC | January 27, 1988 |
| K863429 | wheel checkers | MODIFIED DEVICE FOR SELF EXAMINATION OF EYES | January 20, 1987 |
| K843227 | danek medical | MACULAR FUNCTION ANALYZER | July 22, 1985 |
| K843702 | wheel checkers | APPARATUS & METHODS SELF-EXAM OF EYE | January 3, 1985 |