Product code
QPR: Neurological stimulation for emergency use
FDA product code · Not Classified · Anesthesiology
Key facts
| Product code | QPR |
|---|---|
| Device | Neurological stimulation for emergency use |
| Device class | Not Classified |
| Review panel | Anesthesiology |
| Submission type | EUA - Emergency Use Authorization |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | authorized nerve stimulation devices for respiratory assistance for use during declared public health emergency use. |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- None UDI devices (GUDID)
- None MAUDE adverse event reports
- None Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database