FDA product code EYD: Stirrups
EYD is the FDA product code for stirrups. It is a Class I device, regulated under 21 CFR 876.4890 and reviewed by the Gastroenterology and Urology panel. Devices under EYD reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Stirrups |
| Device class | Class I |
| Regulation | 21 CFR 876.4890 |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Gastroenterology, Urology |
| Premarket route | 510(k) exempt |
Recalls for EYD devices
openFDA lists no recalls for product code EYD.
Frequently asked questions
What is FDA product code EYD?
EYD is the FDA product code for stirrups. It is a Class I device, regulated under 21 CFR 876.4890 and reviewed by the Gastroenterology and Urology panel.
What device class is EYD?
Class I, regulation 21 CFR 876.4890. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code EYD
- Run a recall and safety report across every EYD manufacturer
- Watch product code EYD 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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