FDA product code LNQ: Intestinal Stimulator
LNQ is the FDA product code for intestinal stimulator. It is a HDE device, reviewed by the Gastroenterology and Urology panel. Devices under LNQ reach the market by Unclassified; FDA lists no cleared 510(k)s for it. FDA has posted 1 recall for LNQ devices.
Classification
| Field | Value |
|---|---|
| Device name | Intestinal Stimulator |
| Device class | HDE |
| Review panel | GU — Gastroenterology and Urology |
| Medical specialty | Unknown |
| Premarket route | Unclassified |
Recalls for LNQ devices
1 product recalls in 1 recall events; 0 initiated in the last five years and 0 still open. Most recent: 2009-08-25.
Frequently asked questions
What is FDA product code LNQ?
LNQ is the FDA product code for intestinal stimulator. It is a HDE device, reviewed by the Gastroenterology and Urology panel.
What device class is LNQ?
HDE. Typical premarket route: Unclassified.
Have LNQ devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2009-08-25.
Next steps
- Run an FDA pathway report with predicate devices for product code LNQ
- Run a recall and safety report across every LNQ manufacturer
- Watch product code LNQ 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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