FDA product code HBQ: Instrument, Clip Removal
HBQ is the FDA product code for instrument, clip removal. It is a Class I device, regulated under 21 CFR 882.4200 and reviewed by the Neurology panel. Devices under HBQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Instrument, Clip Removal |
| Device class | Class I |
| Regulation | 21 CFR 882.4200 |
| Review panel | NE — Neurology |
| Medical specialty | Neurology |
| Premarket route | 510(k) exempt |
Recalls for HBQ devices
openFDA lists no recalls for product code HBQ.
Frequently asked questions
What is FDA product code HBQ?
HBQ is the FDA product code for instrument, clip removal. It is a Class I device, regulated under 21 CFR 882.4200 and reviewed by the Neurology panel.
What device class is HBQ?
Class I, regulation 21 CFR 882.4200. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code HBQ
- Run a recall and safety report across every HBQ manufacturer
- Watch product code HBQ 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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