The Metrix Company is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Metrix Company - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
The Metrix Company has 1 FDA 510(k) cleared medical devices. Based in Dubuque, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Metrix Company Filter by specialty or product code using the sidebar.
The Metrix Company — FDA 510(k) Products and Clearance History
1 devices