Product code
QLI: Vaporizer, cder or cber led
FDA product code · Not Classified · Anesthesiology
Key facts
| Product code | QLI |
|---|---|
| Device | Vaporizer, cder or cber led |
| Device class | Not Classified |
| Review panel | Anesthesiology |
| Submission type | Contact ODE |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Vaporizers are products that vaporize and deliver drug substance to the site of action through inhalation route. |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- None UDI devices (GUDID)
- 1–9 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