FDA product code FIK: System, Dialysate Delivery, Recirculating
FIK is the FDA product code for system, dialysate delivery, recirculating. It is a Class II device, regulated under 21 CFR 876.5820 and reviewed by the Gastroenterology and Urology panel. Devices under FIK reach the market by 510(k); FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for FIK devices.
Classification
| Field | Value |
|---|---|
| Device name | System, Dialysate Delivery, Recirculating |
| Device class | Class II |
| Regulation | 21 CFR 876.5820 |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Gastroenterology, Urology |
| Premarket route | 510(k) |
| Life-sustaining or supporting | Yes |
Recalls for FIK devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2014-04-03.
Frequently asked questions
What is FDA product code FIK?
FIK is the FDA product code for system, dialysate delivery, recirculating. It is a Class II device, regulated under 21 CFR 876.5820 and reviewed by the Gastroenterology and Urology panel.
What device class is FIK?
Class II, regulation 21 CFR 876.5820. Typical premarket route: 510(k).
Have FIK devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2014-04-03.
Next steps
- Run an FDA pathway report with predicate devices for product code FIK
- Run a recall and safety report across every FIK manufacturer
- Watch product code FIK 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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