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