FDA product code NFV: Test, Benzodiazepine, Over The Counter
NFV is the FDA product code for test, benzodiazepine, over the counter. It is a Class II device, regulated under 21 CFR 862.3170 and reviewed by the Clinical Toxicology panel. Devices under NFV reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Test, Benzodiazepine, Over The Counter |
| Device class | Class II |
| Regulation | 21 CFR 862.3170 |
| Review panel | TX — Clinical Toxicology |
| Medical specialty | Clinical Toxicology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for NFV devices
openFDA lists no recalls for product code NFV.
Frequently asked questions
What is FDA product code NFV?
NFV is the FDA product code for test, benzodiazepine, over the counter. It is a Class II device, regulated under 21 CFR 862.3170 and reviewed by the Clinical Toxicology panel.
What device class is NFV?
Class II, regulation 21 CFR 862.3170. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NFV
- Run a recall and safety report across every NFV manufacturer
- Watch product code NFV 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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