FDA product code FFW: String And Tubes, Gastrointestinal, To Locate Internal Bleeding
FFW is the FDA product code for string and tubes, gastrointestinal, to locate internal bleeding. It is a Class II device, regulated under 21 CFR 876.5980 and reviewed by the Gastroenterology and Urology panel. Devices under FFW reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | String And Tubes, Gastrointestinal, To Locate Internal Bleeding |
| Device class | Class II |
| Regulation | 21 CFR 876.5980 |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Gastroenterology, Urology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for FFW devices
openFDA lists no recalls for product code FFW.
Frequently asked questions
What is FDA product code FFW?
FFW is the FDA product code for string and tubes, gastrointestinal, to locate internal bleeding. It is a Class II device, regulated under 21 CFR 876.5980 and reviewed by the Gastroenterology and Urology panel.
What device class is FFW?
Class II, regulation 21 CFR 876.5980. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code FFW
- Run a recall and safety report across every FFW manufacturer
- Watch product code FFW 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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