Metritrack, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Metritrack, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hillside, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Metritrack, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
1 devices