FDA product code EWW: Device, Antichoke, Tongs
EWW is the FDA product code for device, antichoke, tongs. It is a Class III device, regulated under 21 CFR 874.5370 and reviewed by the Ear, Nose and Throat panel. Devices under EWW reach the market by PMA; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Device, Antichoke, Tongs |
| Device class | Class III |
| Regulation | 21 CFR 874.5370 |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Ear, Nose, Throat |
| Premarket route | PMA |
Recalls for EWW devices
openFDA lists no recalls for product code EWW.
Frequently asked questions
What is FDA product code EWW?
EWW is the FDA product code for device, antichoke, tongs. It is a Class III device, regulated under 21 CFR 874.5370 and reviewed by the Ear, Nose and Throat panel.
What device class is EWW?
Class III, regulation 21 CFR 874.5370. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code EWW
- Run a recall and safety report across every EWW manufacturer
- Watch product code EWW 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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