HOQ
8 FDA 510(k) clearances · Product code
130 daysmedian time to decision
340 days90th percentile
8clearances measured
FDA profile
- Official device name
- Grid, Amsler
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1330
- Medical specialty
- Ophthalmic
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Alleye (K180895) | Oculocare Medical AG | 2018-06-27 |
| myVision Track Model 005 (K143211) | Vital Art and Science Incorporated | 2015-03-20 |
| MYVISIONTRACK(TM) (K121738) | Vital Art and Science Incorporated | 2013-02-22 |
| MASCULAR COMPUTERIZED PSYCHOPHYSICAL TEST (MCPT) (K014044) | Notal Vision, Inc. | 2002-03-04 |
| KREDA DISC (K874252) | Richmond Products, Inc. | 1988-01-27 |
| MODIFIED DEVICE FOR SELF EXAMINATION OF EYES (K863429) | Wheel Checkers | 1987-01-20 |
| MACULAR FUNCTION ANALYZER (K843227) | Danek Medical, Inc. | 1985-07-22 |
| APPARATUS & METHODS SELF-EXAM OF EYE (K843702) | Wheel Checkers | 1985-01-03 |
Track HOQ automatically
Every clearance here is in the API, with alerts when new ones post.