FDA product code IDD: Alizarin Red
IDD is the FDA product code for alizarin red. It is a Class I device, regulated under 21 CFR 864.1850 and reviewed by the Pathology panel. Devices under IDD reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Alizarin Red |
| Device class | Class I |
| Regulation | 21 CFR 864.1850 |
| Review panel | PA — Pathology |
| Medical specialty | Hematology |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for IDD devices
openFDA lists no recalls for product code IDD.
Frequently asked questions
What is FDA product code IDD?
IDD is the FDA product code for alizarin red. It is a Class I device, regulated under 21 CFR 864.1850 and reviewed by the Pathology panel.
What device class is IDD?
Class I, regulation 21 CFR 864.1850. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code IDD
- Run a recall and safety report across every IDD manufacturer
- Watch product code IDD 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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