FDA product code HZM: Hematoxylin, Acid, Phosphotungstic
HZM is the FDA product code for hematoxylin, acid, phosphotungstic. It is a Class I device, regulated under 21 CFR 864.1850 and reviewed by the Pathology panel. Devices under HZM reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Hematoxylin, Acid, Phosphotungstic |
| 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 HZM devices
openFDA lists no recalls for product code HZM.
Frequently asked questions
What is FDA product code HZM?
HZM is the FDA product code for hematoxylin, acid, phosphotungstic. It is a Class I device, regulated under 21 CFR 864.1850 and reviewed by the Pathology panel.
What device class is HZM?
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 HZM
- Run a recall and safety report across every HZM manufacturer
- Watch product code HZM 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.