FDA product code IMQ: Attachment, Narrowing, Wheelchair
IMQ is the FDA product code for attachment, narrowing, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel. Devices under IMQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Attachment, Narrowing, 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 IMQ devices
openFDA lists no recalls for product code IMQ.
Frequently asked questions
What is FDA product code IMQ?
IMQ is the FDA product code for attachment, narrowing, wheelchair. It is a Class I device, regulated under 21 CFR 890.3920 and reviewed by the Physical Medicine panel.
What device class is IMQ?
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 IMQ
- Run a recall and safety report across every IMQ manufacturer
- Watch product code IMQ 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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