FDA product code MPQ: Container, Specimen, Urine, Drugs Of Abuse, Over The Counter
MPQ is the FDA product code for container, specimen, urine, drugs of abuse, over the counter. It is a Class I device, regulated under 21 CFR 864.3260 and reviewed by the Clinical Chemistry panel. Devices under MPQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Container, Specimen, Urine, Drugs Of Abuse, Over The Counter |
| Device class | Class I |
| Regulation | 21 CFR 864.3260 |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Pathology |
| Premarket route | 510(k) exempt |
Recalls for MPQ devices
openFDA lists no recalls for product code MPQ.
Frequently asked questions
What is FDA product code MPQ?
MPQ is the FDA product code for container, specimen, urine, drugs of abuse, over the counter. It is a Class I device, regulated under 21 CFR 864.3260 and reviewed by the Clinical Chemistry panel.
What device class is MPQ?
Class I, regulation 21 CFR 864.3260. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code MPQ
- Run a recall and safety report across every MPQ manufacturer
- Watch product code MPQ 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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