FDA product code INC: Cuff, Pusher, Wheelchair
INC is the FDA product code for cuff, pusher, wheelchair. It is a Class I device, regulated under 21 CFR 890.3910 and reviewed by the Physical Medicine panel. Devices under INC reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Cuff, Pusher, Wheelchair |
| Device class | Class I |
| Regulation | 21 CFR 890.3910 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for INC devices
openFDA lists no recalls for product code INC.
Frequently asked questions
What is FDA product code INC?
INC is the FDA product code for cuff, pusher, wheelchair. It is a Class I device, regulated under 21 CFR 890.3910 and reviewed by the Physical Medicine panel.
What device class is INC?
Class I, regulation 21 CFR 890.3910. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code INC
- Run a recall and safety report across every INC manufacturer
- Watch product code INC 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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