Diatron U.S., Inc. is one of 4860 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diatron U.S., Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Diatron U.S., Inc. has 3 FDA 510(k) cleared medical devices. Based in Lenexa, US.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Diatron U.S., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diatron U.S., Inc.
3 devices