Microsoft Corp. is one of 14040 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microsoft Corp. - FDA 510(k) Cleared Devices
Recent clearances: Radiomics App v1.0, MICROSOFT AMALGA UIS IMAGE PROCESSING MODULE
2
Total
2
Cleared
0
Denied
Microsoft Corp., is a global technology company with a manufacturing facility in Austin, US. The company has developed software and imaging solutions for healthcare applications.
Microsoft holds 2 FDA 510(k) clearances from 2 total submissions. The company specializes in Radiology devices, with clearances spanning from 2012 to 2017. This regulatory record reflects the company's historical involvement in medical imaging technology.
Activity status: inactive. No new clearances have been granted in more than five years. This profile serves as a historical record of the company's past FDA 510(k) submissions and cleared devices in the radiology sector.
Explore the complete clearance history, device names, product codes, and approval dates in the full regulatory database.
510(k) submissions have been managed by Biologics Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Microsoft Corp.
2 devices