FDA product code NNQ: Forceps, Wire Closure, Ent, Non-Sterile
NNQ is the FDA product code for forceps, wire closure, ent, non-sterile. It is a Class I device, regulated under 21 CFR 874.3540 and reviewed by the Ear, Nose and Throat panel. Devices under NNQ reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it.
Definition
Prosthesis modification instrument for ossicular replacement surgery; see product code JXX.
Classification
| Field | Value |
|---|---|
| Device name | Forceps, Wire Closure, Ent, Non-Sterile |
| Device class | Class I |
| Regulation | 21 CFR 874.3540 |
| Review panel | EN — Ear, Nose and Throat |
| Medical specialty | Ear, Nose, Throat |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Recalls for NNQ devices
openFDA lists no recalls for product code NNQ.
Frequently asked questions
What is FDA product code NNQ?
NNQ is the FDA product code for forceps, wire closure, ent, non-sterile. It is a Class I device, regulated under 21 CFR 874.3540 and reviewed by the Ear, Nose and Throat panel.
What device class is NNQ?
Class I, regulation 21 CFR 874.3540. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code NNQ
- Run a recall and safety report across every NNQ manufacturer
- Watch product code NNQ 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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