FDA product code MWG: System, Oxygen, Aqueous
MWG is the FDA product code for system, oxygen, aqueous. It is a Class III device, reviewed by the Cardiovascular panel. Devices under MWG 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 | System, Oxygen, Aqueous |
| Device class | Class III |
| Review panel | CV — Cardiovascular |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for MWG devices
openFDA lists no recalls for product code MWG.
Frequently asked questions
What is FDA product code MWG?
MWG is the FDA product code for system, oxygen, aqueous. It is a Class III device, reviewed by the Cardiovascular panel.
What device class is MWG?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code MWG
- Run a recall and safety report across every MWG manufacturer
- Watch product code MWG 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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