Mriglobal is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mriglobal - FDA 510(k) Cleared Devices
Recent clearances: Applied Biosystems Bacillus anthracis Detection Kit
1
Total
1
Cleared
0
Denied
Mriglobal has 1 FDA 510(k) cleared medical devices. Based in Kansas City, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Mriglobal Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MDC Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mriglobal
1 devices