FDA product code QOX: Multi-Patient Circuit Connector
QOX is the FDA product code for multi-patient circuit connector. It is a Not classified device, reviewed by the Ear, Nose and Throat panel. Devices under QOX reach the market by PMA; FDA lists no cleared 510(k)s for it.
Definition
Accessory to single patient ventilator to allow multi-patient ventilation during declared public health emergency
Classification
| Field | Value |
|---|---|
| Device name | Multi-Patient Circuit Connector |
| Device class | Not classified |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for QOX devices
openFDA lists no recalls for product code QOX.
Frequently asked questions
What is FDA product code QOX?
QOX is the FDA product code for multi-patient circuit connector. It is a Not classified device, reviewed by the Ear, Nose and Throat panel.
What device class is QOX?
Not classified. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QOX
- Run a recall and safety report across every QOX manufacturer
- Watch product code QOX 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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