Narnar, LLC
Country not established
- Devices
- 1
What Narnar, LLC makes
Narnar, LLC manufactures the GECHO, a medical device designed for diagnostic imaging of the gastrointestinal tract, likely utilizing endoscopic ultrasound technology for internal organ visualization.
The GECHO is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Gecho Ref K250120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Narnar, LLC have in the registry?
The registry currently lists 1 device for Narnar, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Narnar, LLC's devices?
Among its 1 most recently registered device, Narnar, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Narnar, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Narnar, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Narnar, LLC in the registry?
The most recently registered devices listed for Narnar, LLC include GECHO.