FDA product code FNS: Ring Cutter
FNS is the FDA product code for ring cutter. It is a Class I device, regulated under 21 CFR 880.6200 and reviewed by the General Hospital panel. Devices under FNS reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Ring Cutter |
| Device class | Class I |
| Regulation | 21 CFR 880.6200 |
| Review panel | HO — General Hospital |
| Medical specialty | General Hospital |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for FNS devices
openFDA lists no recalls for product code FNS.
Frequently asked questions
What is FDA product code FNS?
FNS is the FDA product code for ring cutter. It is a Class I device, regulated under 21 CFR 880.6200 and reviewed by the General Hospital panel.
What device class is FNS?
Class I, regulation 21 CFR 880.6200. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code FNS
- Run a recall and safety report across every FNS manufacturer
- Watch product code FNS 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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