HOJ
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Screen, Tangent, Target
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1810
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TANGENT SCREEN (K873919) | Richmond Products, Inc. | 1987-10-28 |
| SPECTABLE FRAME MAGNIFYING BRILLETTE (K844657) | Pro Design Intl. AS | 1984-12-11 |
| CHART PROJECTOR (K821081) | Medical Equipment Designs, Inc. | 1982-06-14 |
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