FDA product code NQV: Catheter, Suction, Tracheobronchial, Reprocessed
NQV is the FDA product code for catheter, suction, tracheobronchial, reprocessed. It is a Class I device, regulated under 21 CFR 876.4680 and reviewed by the Anesthesiology panel. Devices under NQV reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Definition
A tracheobronchial suction catheter is a device used to aspirate liquids or semisolids from a patient's upper airway. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Classification
| Field | Value |
|---|---|
| Device name | Catheter, Suction, Tracheobronchial, Reprocessed |
| Device class | Class I |
| Regulation | 21 CFR 876.4680 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Gastroenterology, Urology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for NQV devices
openFDA lists no recalls for product code NQV.
Frequently asked questions
What is FDA product code NQV?
NQV is the FDA product code for catheter, suction, tracheobronchial, reprocessed. It is a Class I device, regulated under 21 CFR 876.4680 and reviewed by the Anesthesiology panel.
What device class is NQV?
Class I, regulation 21 CFR 876.4680. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NQV
- Run a recall and safety report across every NQV manufacturer
- Watch product code NQV 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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