FDA product code OAA: Aid, Visual, For Nausea
OAA is the FDA product code for aid, visual, for nausea. It is a Not classified device, reviewed by the Ear, Nose and Throat panel. Devices under OAA reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
To relieve the symptoms associated with motion sickness.
Classification
| Field | Value |
|---|---|
| Device name | Aid, Visual, For Nausea |
| Device class | Not classified |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Unknown |
| Premarket route | 510(k) exempt |
Recalls for OAA devices
openFDA lists no recalls for product code OAA.
Frequently asked questions
What is FDA product code OAA?
OAA is the FDA product code for aid, visual, for nausea. It is a Not classified device, reviewed by the Ear, Nose and Throat panel.
What device class is OAA?
Not classified. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code OAA
- Run a recall and safety report across every OAA manufacturer
- Watch product code OAA 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.
All Ear, Nose and Throat product codes · FDA product code lookup