FDA product code KHY: Cane, Safety Walk
KHY is the FDA product code for cane, safety walk. It is a Class I device, regulated under 21 CFR 890.3075 and reviewed by the Physical Medicine panel. Devices under KHY reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for KHY devices.
Classification
| Field | Value |
|---|---|
| Device name | Cane, Safety Walk |
| Device class | Class I |
| Regulation | 21 CFR 890.3075 |
| Review panel | PM — Physical Medicine |
| Medical specialty | Physical Medicine |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for KHY devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2012-11-06.
Frequently asked questions
What is FDA product code KHY?
KHY is the FDA product code for cane, safety walk. It is a Class I device, regulated under 21 CFR 890.3075 and reviewed by the Physical Medicine panel.
What device class is KHY?
Class I, regulation 21 CFR 890.3075. Typical premarket route: 510(k) exempt.
Have KHY devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2012-11-06.
Next steps
- Run an FDA pathway report with predicate devices for product code KHY
- Run a recall and safety report across every KHY manufacturer
- Watch product code KHY 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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