FDA product code QOQ: Non-Continuous Ventilator For Emergency Use
QOQ is the FDA product code for non-continuous ventilator for emergency use. It is a Not classified device, reviewed by the Anesthesiology panel. Devices under QOQ reach the market by PMA; FDA lists no cleared 510(k)s for it.
Definition
A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing for use during declared public health emergency.
Classification
| Field | Value |
|---|---|
| Device name | Non-Continuous Ventilator For Emergency Use |
| Device class | Not classified |
| Review panel | AN — Anesthesiology |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for QOQ devices
openFDA lists no recalls for product code QOQ.
HCPCS codes with matching descriptors
Text match between the FDA device name and CMS descriptors, not an official crosswalk:
- J0888 — Injection, epoetin beta, 1 microgram, (for non esrd use)
- J0881 — Injection, darbepoetin alfa, 1 microgram (non-esrd use)
Frequently asked questions
What is FDA product code QOQ?
QOQ is the FDA product code for non-continuous ventilator for emergency use. It is a Not classified device, reviewed by the Anesthesiology panel.
What device class is QOQ?
Not classified. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QOQ
- Run a recall and safety report across every QOQ manufacturer
- Watch product code QOQ 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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