FDA product code MRQ: Analyzer, Nitrogen Dioxide
MRQ is the FDA product code for analyzer, nitrogen dioxide. It is a Class II device, regulated under 21 CFR 868.2385 and reviewed by the Anesthesiology panel. Devices under MRQ reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Analyzer, Nitrogen Dioxide |
| Device class | Class II |
| Regulation | 21 CFR 868.2385 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Anesthesiology |
| Premarket route | 510(k) |
| Life-sustaining or supporting | Yes |
| Third-party 510(k) review eligible | Yes |
Recalls for MRQ devices
openFDA lists no recalls for product code MRQ.
Frequently asked questions
What is FDA product code MRQ?
MRQ is the FDA product code for analyzer, nitrogen dioxide. It is a Class II device, regulated under 21 CFR 868.2385 and reviewed by the Anesthesiology panel.
What device class is MRQ?
Class II, regulation 21 CFR 868.2385. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code MRQ
- Run a recall and safety report across every MRQ manufacturer
- Watch product code MRQ 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.