FDA product code QPR: Neurological Stimulation For Emergency Use
QPR is the FDA product code for neurological stimulation for emergency use. It is a Not classified device, reviewed by the Anesthesiology panel. Devices under QPR reach the market by PMA; FDA lists no cleared 510(k)s for it.
Definition
authorized nerve stimulation devices for respiratory assistance for use during declared public health emergency use.
Classification
| Field | Value |
|---|---|
| Device name | Neurological Stimulation For Emergency Use |
| Device class | Not classified |
| Review panel | AN — Anesthesiology |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for QPR devices
openFDA lists no recalls for product code QPR.
Frequently asked questions
What is FDA product code QPR?
QPR is the FDA product code for neurological stimulation for emergency use. It is a Not classified device, reviewed by the Anesthesiology panel.
What device class is QPR?
Not classified. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QPR
- Run a recall and safety report across every QPR manufacturer
- Watch product code QPR 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.