Sterisson
Country not established
- Devices
- 1
What Sterisson makes
Sterisson manufactures an ultrasonic medical device, specifically the Model 3 LO 4, designed for medical applications requiring ultrasound technology.
The Model 3 LO 4 is listed under the FDA’s 510(k) pathway as a Class II device. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ultrasonic Medical Device Model 3 Lo 4 Ref K827708
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sterisson have in the registry?
The registry currently lists 1 device for Sterisson. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterisson's devices?
Among its 1 most recently registered device, Sterisson has devices listed in FDA 510(k) (1 device).
What are the newest devices from Sterisson in the registry?
The most recently registered devices listed for Sterisson include ULTRASONIC MEDICAL DEVICE MODEL 3 LO 4.