FDA product code OAQ: Electronic Media, Hyperacusis
OAQ is the FDA product code for electronic media, hyperacusis. It is a Not classified device, reviewed by the Ear, Nose and Throat panel. Devices under OAQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
To improve sound tolerances.
Classification
| Field | Value |
|---|---|
| Device name | Electronic Media, Hyperacusis |
| Device class | Not classified |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Unknown |
| Premarket route | 510(k) exempt |
Recalls for OAQ devices
openFDA lists no recalls for product code OAQ.
Frequently asked questions
What is FDA product code OAQ?
OAQ is the FDA product code for electronic media, hyperacusis. It is a Not classified device, reviewed by the Ear, Nose and Throat panel.
What device class is OAQ?
Not classified. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code OAQ
- Run a recall and safety report across every OAQ manufacturer
- Watch product code OAQ 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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