FDA product code IMZ: Holder, Crutch And Cane, Wheelchair
IMZ is the FDA product code for holder, crutch and cane, wheelchair. It is a Class I device, regulated under 21 CFR 890.3910 and reviewed by the Physical Medicine panel. Devices under IMZ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Holder, Crutch And Cane, 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 IMZ devices
openFDA lists no recalls for product code IMZ.
Frequently asked questions
What is FDA product code IMZ?
IMZ is the FDA product code for holder, crutch and cane, wheelchair. It is a Class I device, regulated under 21 CFR 890.3910 and reviewed by the Physical Medicine panel.
What device class is IMZ?
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 IMZ
- Run a recall and safety report across every IMZ manufacturer
- Watch product code IMZ 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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