FDA product code EYH: Table, Cysto, Non-Electrical
EYH is the FDA product code for table, cysto, non-electrical. It is a Class I device, regulated under 21 CFR 876.4890 and reviewed by the Gastroenterology and Urology panel. Devices under EYH reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Table, Cysto, Non-Electrical |
| 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 EYH devices
openFDA lists no recalls for product code EYH.
Frequently asked questions
What is FDA product code EYH?
EYH is the FDA product code for table, cysto, non-electrical. It is a Class I device, regulated under 21 CFR 876.4890 and reviewed by the Gastroenterology and Urology panel.
What device class is EYH?
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 EYH
- Run a recall and safety report across every EYH manufacturer
- Watch product code EYH 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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