FDA product code QVG: Embolization Agent, Vascular
QVG is the FDA product code for embolization agent, vascular. It is a Class III device, reviewed by the Cardiovascular panel. Devices under QVG reach the market by PMA; FDA lists no cleared 510(k)s for it. 2 PMA applications cite this product code.
Definition
For occluding peripheral vessels
Classification
| Field | Value |
|---|---|
| Device name | Embolization Agent, Vascular |
| Device class | Class III |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | PMA |
| Implant | Yes |
Recalls for QVG devices
openFDA lists no recalls for product code QVG.
Frequently asked questions
What is FDA product code QVG?
QVG is the FDA product code for embolization agent, vascular. It is a Class III device, reviewed by the Cardiovascular panel.
What device class is QVG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QVG
- Run a recall and safety report across every QVG manufacturer
- Watch product code QVG 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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