FDA product code EPG: Stimulator, Transdermal
EPG is the FDA product code for stimulator, transdermal. It is a Class III device, reviewed by the Ear, Nose and Throat panel. Devices under EPG reach the market by PMA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Stimulator, Transdermal |
| Device class | Class III |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for EPG devices
openFDA lists no recalls for product code EPG.
Frequently asked questions
What is FDA product code EPG?
EPG is the FDA product code for stimulator, transdermal. It is a Class III device, reviewed by the Ear, Nose and Throat panel.
What device class is EPG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code EPG
- Run a recall and safety report across every EPG manufacturer
- Watch product code EPG 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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