Deepecho
Country not established
- Devices
- 1
What Deepecho makes
Deepecho manufactures ultrasound imaging devices, specifically the DEEPECHO system, designed for medical imaging applications.
The DEEPECHO system is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Deepecho Ref K242594
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deepecho have in the registry?
The registry currently lists 1 device for Deepecho. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deepecho's devices?
Among its 1 most recently registered device, Deepecho has devices listed in FDA 510(k) (1 device).
What risk classes do Deepecho's devices fall under?
Among its 1 most recently registered device, the classes recorded for Deepecho's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deepecho in the registry?
The most recently registered devices listed for Deepecho include DEEPECHO.