FDA product code MQT: Pump, Drug Administration, Closed Loop
MQT is the FDA product code for pump, drug administration, closed loop. It is a Class III device, reviewed by the General Hospital panel. Devices under MQT reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Pump, Drug Administration, Closed Loop |
| Device class | Class III |
| Review panel | HO — General Hospital |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MQT devices
openFDA lists no recalls for product code MQT.
Frequently asked questions
What is FDA product code MQT?
MQT is the FDA product code for pump, drug administration, closed loop. It is a Class III device, reviewed by the General Hospital panel.
What device class is MQT?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MQT
- Run a recall and safety report across every MQT manufacturer
- Watch product code MQT 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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