Metritrack, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Metritrack, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Breast Volume Navigator (BVN) Model G-2000
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.
FDA 510(k) Regulatory Record - Metritrack, Inc.
1 devices