FDA product code DOO: Liquid Chromatography, Phenobarbital
DOO is the FDA product code for liquid chromatography, phenobarbital. It is a Class II device, regulated under 21 CFR 862.3660 and reviewed by the Clinical Toxicology panel. Devices under DOO reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Liquid Chromatography, Phenobarbital |
| Device class | Class II |
| Regulation | 21 CFR 862.3660 |
| Review panel | TX — Clinical Toxicology |
| Medical specialty | Clinical Toxicology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for DOO devices
openFDA lists no recalls for product code DOO.
Frequently asked questions
What is FDA product code DOO?
DOO is the FDA product code for liquid chromatography, phenobarbital. It is a Class II device, regulated under 21 CFR 862.3660 and reviewed by the Clinical Toxicology panel.
What device class is DOO?
Class II, regulation 21 CFR 862.3660. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code DOO
- Run a recall and safety report across every DOO manufacturer
- Watch product code DOO 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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