FDA product code HDI: Hook, Destructive, Obstetrical
HDI is the FDA product code for hook, destructive, obstetrical. It is a Class II device, regulated under 21 CFR 884.4500 and reviewed by the Obstetrics and Gynecology panel. Devices under HDI reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Hook, Destructive, Obstetrical |
| Device class | Class II |
| Regulation | 21 CFR 884.4500 |
| Review panel | OB — Obstetrics and Gynecology |
| Medical specialty | Obstetrics/Gynecology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for HDI devices
openFDA lists no recalls for product code HDI.
Frequently asked questions
What is FDA product code HDI?
HDI is the FDA product code for hook, destructive, obstetrical. It is a Class II device, regulated under 21 CFR 884.4500 and reviewed by the Obstetrics and Gynecology panel.
What device class is HDI?
Class II, regulation 21 CFR 884.4500. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code HDI
- Run a recall and safety report across every HDI manufacturer
- Watch product code HDI 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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