FDA product code QLI: Vaporizer, Cder Or Cber Led
QLI is the FDA product code for vaporizer, cder or cber led. It is a Not classified device, reviewed by the Anesthesiology panel. Devices under QLI reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Vaporizers are products that vaporize and deliver drug substance to the site of action through inhalation route.
Classification
| Field | Value |
|---|---|
| Device name | Vaporizer, Cder Or Cber Led |
| Device class | Not classified |
| Review panel | AN — Anesthesiology |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for QLI devices
openFDA lists no recalls for product code QLI.
Frequently asked questions
What is FDA product code QLI?
QLI is the FDA product code for vaporizer, cder or cber led. It is a Not classified device, reviewed by the Anesthesiology panel.
What device class is QLI?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code QLI
- Run a recall and safety report across every QLI manufacturer
- Watch product code QLI 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.