FDA product code HJD: Illuminator, Color Vision Plate
HJD is the FDA product code for illuminator, color vision plate. It is a Class I device, regulated under 21 CFR 886.1160 and reviewed by the Ophthalmic panel. FDA has cleared 1 510(k) submission under HJD. The average 510(k) review took 68 days (median 68).
Classification
| Field | Value |
|---|---|
| Device name | Illuminator, Color Vision Plate |
| Device class | Class I |
| Regulation | 21 CFR 886.1160 |
| Review panel | OP — Ophthalmic |
| Medical specialty | Ophthalmic |
| Premarket route | 510(k) exempt |
Compare with all 510(k) review times · Search every HJD clearance
Top HJD applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Richmond Products, Inc. | 1 | 1987-12-02 |
Most recent HJD clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K873913 | Richmond Products, Inc. | COLOR BOOK ILLUMINATOR STAND | 1987-12-02 | 68 |
Recalls for HJD devices
openFDA lists no recalls for product code HJD.
Frequently asked questions
What is FDA product code HJD?
HJD is the FDA product code for illuminator, color vision plate. It is a Class I device, regulated under 21 CFR 886.1160 and reviewed by the Ophthalmic panel.
What device class is HJD?
Class I, regulation 21 CFR 886.1160. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code HJD?
Across 1 cleared submissions the average was 68 days from receipt to decision (median 68).
Which companies have the most HJD clearances?
Richmond Products, Inc. (1).
Next steps
- Run an FDA pathway report with predicate devices for product code HJD
- Run a recall and safety report across every HJD manufacturer
- Watch product code HJD 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.
All Ophthalmic product codes · FDA product code lookup · 510(k) database search · 510(k) review times