Metritrack, LLC is one of 19060 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Metritrack, LLC - FDA 510(k) Cleared Devices
Recent clearances: BREAST VOLUME NAVIGATOR
1
Total
1
Cleared
0
Denied
Metritrack, LLC has 1 FDA 510(k) cleared medical devices. Based in Hillside, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Metritrack, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Metritrack, LLC
1 devices