FDA product code QIZ: Material, Implantable For Controlled Release, Cder Or Cber Led
QIZ is the FDA product code for material, implantable for controlled release, cder or cber led. It is a Not classified device, reviewed by the General Hospital panel. Devices under QIZ reach the market by Contact FDA; FDA lists no cleared 510(k)s for it.
Definition
Implantable material for controlled release of drug substance.
Classification
| Field | Value |
|---|---|
| Device name | Material, Implantable For Controlled Release, Cder Or Cber Led |
| Device class | Not classified |
| Review panel | HO — General Hospital |
| Medical specialty | Unknown |
| Premarket route | Contact FDA |
Recalls for QIZ devices
openFDA lists no recalls for product code QIZ.
Frequently asked questions
What is FDA product code QIZ?
QIZ is the FDA product code for material, implantable for controlled release, cder or cber led. It is a Not classified device, reviewed by the General Hospital panel.
What device class is QIZ?
Not classified. Typical premarket route: Contact FDA.
Next steps
- Run an FDA pathway report with predicate devices for product code QIZ
- Run a recall and safety report across every QIZ manufacturer
- Watch product code QIZ 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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