FDA product code QUB: Suction Lipoplasty System For Removal And Transfer
QUB is the FDA product code for suction lipoplasty system for removal and transfer. It is a Class II device, regulated under 21 CFR 878.5040 and reviewed by the General and Plastic Surgery panel. Devices under QUB reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Definition
Removal and transfer/reimplantation of autologous adipose tissue without further manipulation for aesthetic body contouring
Classification
| Field | Value |
|---|---|
| Device name | Suction Lipoplasty System For Removal And Transfer |
| Device class | Class II |
| Regulation | 21 CFR 878.5040 |
| Review panel | SU — General and Plastic Surgery |
| Medical specialty | General, Plastic Surgery |
| Premarket route | 510(k) |
Recalls for QUB devices
openFDA lists no recalls for product code QUB.
Frequently asked questions
What is FDA product code QUB?
QUB is the FDA product code for suction lipoplasty system for removal and transfer. It is a Class II device, regulated under 21 CFR 878.5040 and reviewed by the General and Plastic Surgery panel.
What device class is QUB?
Class II, regulation 21 CFR 878.5040. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code QUB
- Run a recall and safety report across every QUB manufacturer
- Watch product code QUB 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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