FDA product code EYI: Adaptor, Ureteral Catheter
EYI is the FDA product code for adaptor, ureteral catheter. It is a Class I device, regulated under 21 CFR 876.5130 and reviewed by the Gastroenterology and Urology panel. Devices under EYI reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Adaptor, Ureteral Catheter |
| Device class | Class I |
| Regulation | 21 CFR 876.5130 |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Gastroenterology, Urology |
| Premarket route | 510(k) exempt |
Recalls for EYI devices
openFDA lists no recalls for product code EYI.
Frequently asked questions
What is FDA product code EYI?
EYI is the FDA product code for adaptor, ureteral catheter. It is a Class I device, regulated under 21 CFR 876.5130 and reviewed by the Gastroenterology and Urology panel.
What device class is EYI?
Class I, regulation 21 CFR 876.5130. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code EYI
- Run a recall and safety report across every EYI manufacturer
- Watch product code EYI 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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