FDA product code NCT: Instrument, Glucose, Noninvasive Technology
NCT is the FDA product code for instrument, glucose, noninvasive technology. It is a Class III device, reviewed by the Clinical Chemistry panel. Devices under NCT reach the market by PMA; FDA lists no cleared 510(k)s for it. 1 PMA application cites this product code.
Classification
| Field | Value |
|---|---|
| Device name | Instrument, Glucose, Noninvasive Technology |
| Device class | Class III |
| Review panel | CH — Clinical Chemistry |
| Medical specialty | Unknown |
| Premarket route | PMA |
Recalls for NCT devices
openFDA lists no recalls for product code NCT.
Frequently asked questions
What is FDA product code NCT?
NCT is the FDA product code for instrument, glucose, noninvasive technology. It is a Class III device, reviewed by the Clinical Chemistry panel.
What device class is NCT?
Class III. Typical premarket route: PMA.
Next steps
- Run an FDA pathway report with predicate devices for product code NCT
- Run a recall and safety report across every NCT manufacturer
- Watch product code NCT 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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