Microsoft Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Microsoft Corp. makes
Microsoft Corp. develops image processing modules and radiomics software tools designed for medical imaging analysis, including the Amalga UIS Image Processing Module and Radiomics App v1.0. These tools are intended to assist in the interpretation and analysis of medical images, supporting diagnostic workflows.
The company’s portfolio is regulated as Class II medical devices in the U.S. and is listed under FDA 510(k) submissions. The devices are based in the United States.
Catalogue
Microsoft Amalga Uis Image Processing Module Ref K120734
Regimes: 510(k) Registry: 510(k)Radiomics App v1.0 Ref K173420
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microsoft Corp. have in the registry?
The registry currently lists 2 devices for Microsoft Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microsoft Corp.'s devices?
Among its 2 most recently registered devices, Microsoft Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Microsoft Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Microsoft Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microsoft Corp. in the registry?
The most recently registered devices listed for Microsoft Corp. include MICROSOFT AMALGA UIS IMAGE PROCESSING MODULE and Radiomics App v1.0.