FDA product code NZF: Static Electricity-Emitting Device, Cosmetic Use
NZF is the FDA product code for static electricity-emitting device, cosmetic use. It is a Not classified device, reviewed by the General and Plastic Surgery panel. Devices under NZF reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
Intended for relaxation and cosmetic use.
Classification
| Field | Value |
|---|---|
| Device name | Static Electricity-Emitting Device, Cosmetic Use |
| Device class | Not classified |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | Unknown |
| Premarket route | 510(k) exempt |
Recalls for NZF devices
openFDA lists no recalls for product code NZF.
Frequently asked questions
What is FDA product code NZF?
NZF is the FDA product code for static electricity-emitting device, cosmetic use. It is a Not classified device, reviewed by the General and Plastic Surgery panel.
What device class is NZF?
Not classified. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code NZF
- Run a recall and safety report across every NZF manufacturer
- Watch product code NZF 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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