Neomatrix, LLC
Country not established
- Devices
- 1
What Neomatrix, LLC makes
Neomatrix, LLC manufactures the NAFD 100, a medical device designed for non-invasive atrial fibrillation detection.
The NAFD 100 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Nafd 100 Ref K020848
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neomatrix, LLC have in the registry?
The registry currently lists 1 device for Neomatrix, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neomatrix, LLC's devices?
Among its 1 most recently registered device, Neomatrix, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Neomatrix, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Neomatrix, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neomatrix, LLC in the registry?
The most recently registered devices listed for Neomatrix, LLC include NAFD 100.