Diotech CO is one of 4783 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diotech CO - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Diotech CO has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Diotech CO Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diotech CO
2 devices