Diatron Group is one of 4981 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diatron Group - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Diatron Group has 2 FDA 510(k) cleared medical devices. Based in Westo, US.
Historical record: 2 cleared submissions from 2011 to 2020. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diatron Group Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ammirati Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Diatron Group
2 devices