FDA Product Code
FDA Product Code HOQ — Clearance Directory
- Device Class
- Class I
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.1330
510(k) Clearances — 8 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K180895 | Alleye | Oculocare Medical AG | 2018-06-27 | Traditional | PDF ↗ |
| K143211 | myVision Track Model 005 | Vital Art and Science Incorporated | 2015-03-20 | Traditional | PDF ↗ |
| K121738 | MYVISIONTRACK(TM) | Vital Art and Science Incorporated | 2013-02-22 | Traditional | PDF ↗ |
| K014044 | MASCULAR COMPUTERIZED PSYCHOPHYSICAL TEST (MCPT) | Notal Vision, Inc. | 2002-03-04 | Traditional | PDF ↗ |
| K874252 | KREDA DISC | Richmond Products, Inc. | 1988-01-27 | Traditional | PDF ↗ |
| K863429 | MODIFIED DEVICE FOR SELF EXAMINATION OF EYES | Wheel Checkers | 1987-01-20 | Traditional | PDF ↗ |
| K843227 | MACULAR FUNCTION ANALYZER | Danek Medical, Inc. | 1985-07-22 | Traditional | PDF ↗ |
| K843702 | APPARATUS & METHODS SELF-EXAM OF EYE | Wheel Checkers | 1985-01-03 | Traditional | PDF ↗ |
Product code HOQ · Class I · Ophthalmic. Data: openFDA.