FDA product code HOJ: Screen, Tangent, Target
HOJ is the FDA product code for screen, tangent, target. It is a Class I device, regulated under 21 CFR 886.1810 and reviewed by the Ophthalmic panel. FDA has cleared 3 510(k) submissions under HOJ, from 3 different applicants. The average 510(k) review took 34 days (median 33).
Classification
| Field | Value |
|---|---|
| Device name | Screen, Tangent, Target |
| Device class | Class I |
| Regulation | 21 CFR 886.1810 |
| Review panel | OP — Ophthalmic |
| Medical specialty | Ophthalmic |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every HOJ clearance
Top HOJ applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Richmond Products, Inc. | 1 | 1987-10-28 |
| Pro Design Intl. AS | 1 | 1984-12-11 |
| Medical Equipment Designs, Inc. | 1 | 1982-06-14 |
Most recent HOJ clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K873919 | Richmond Products, Inc. | TANGENT SCREEN | 1987-10-28 | 33 |
| K844657 | Pro Design Intl. AS | SPECTABLE FRAME MAGNIFYING BRILLETTE | 1984-12-11 | 12 |
| K821081 | Medical Equipment Designs, Inc. | CHART PROJECTOR | 1982-06-14 | 56 |
Recalls for HOJ devices
openFDA lists no recalls for product code HOJ.
Frequently asked questions
What is FDA product code HOJ?
HOJ is the FDA product code for screen, tangent, target. It is a Class I device, regulated under 21 CFR 886.1810 and reviewed by the Ophthalmic panel.
What device class is HOJ?
Class I, regulation 21 CFR 886.1810. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code HOJ?
Across 3 cleared submissions the average was 34 days from receipt to decision (median 33).
Which companies have the most HOJ clearances?
Richmond Products, Inc. (1); Pro Design Intl. AS (1); Medical Equipment Designs, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code HOJ
- Run a recall and safety report across every HOJ manufacturer
- Watch product code HOJ for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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