Medical Device Manufacturer · US , Westo , FL

Diatron Group - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2011

Total

Cleared

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: Toxicology.

Browse the FDA 510(k) cleared devices submitted by Diatron Group Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Diatron Group

2 devices

1-2 of 2