FDA product code IMN: Climber, Curb, Wheelchair
IMN is the FDA product code for climber, curb, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel. Devices under IMN reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Climber, Curb, Wheelchair |
| Device class | Class I |
| Regulation | 21 CFR 890.3920 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
Recalls for IMN devices
openFDA lists no recalls for product code IMN.
Frequently asked questions
What is FDA product code IMN?
IMN is the FDA product code for climber, curb, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel.
What device class is IMN?
Class I, regulation 21 CFR 890.3920. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code IMN
- Run a recall and safety report across every IMN manufacturer
- Watch product code IMN 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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