FDA product code QOD: Extracorporeal Circuit And Accessories For Long Term Respiratory Cariodpulmonary Failure
QOD is the FDA product code for extracorporeal circuit and accessories for long term respiratory cariodpulmonary failure. It is a Not classified device, reviewed by the Cardiovascular panel. Devices under QOD reach the market by PMA; FDA lists no cleared 510(k)s for it.
Definition
Extracorporeal circuit and accessories for long-term respiratory/cardiopulmonary failure for patient having cardiopulmonary failure during the declared public health emergency.
Classification
| Field | Value |
|---|---|
| Device name | Extracorporeal Circuit And Accessories For Long Term Respiratory Cariodpulmonary Failure |
| Device class | Not classified |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for QOD devices
openFDA lists no recalls for product code QOD.
Frequently asked questions
What is FDA product code QOD?
QOD is the FDA product code for extracorporeal circuit and accessories for long term respiratory cariodpulmonary failure. It is a Not classified device, reviewed by the Cardiovascular panel.
What device class is QOD?
Not classified. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code QOD
- Run a recall and safety report across every QOD manufacturer
- Watch product code QOD 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.