Instrument Ab Scanditronix
Country not established
- Devices
- 1
What Instrument Ab Scanditronix makes
Instrument AB Scanditronix manufactures the MM-22 Microtron, a medical device designed for radiation therapy applications, specifically delivering precise microbeam radiation doses.
The MM-22 Microtron is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mm-22 Microtron Ref K827704
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Instrument AB Scanditronix have in the registry?
The registry currently lists 1 device for Instrument AB Scanditronix. Devices recorded under merged duplicate company entries are counted once.
Which registries list Instrument AB Scanditronix's devices?
Among its 1 most recently registered device, Instrument AB Scanditronix has devices listed in FDA 510(k) (1 device).
What are the newest devices from Instrument AB Scanditronix in the registry?
The most recently registered devices listed for Instrument AB Scanditronix include MM-22 MICROTRON.