Diatron U.S., Inc. is one of 13015 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
Recent clearances: Diatron Pictus 700 Clinical Chemistry Analyzer, Diatron ISE, Diatron Glucose Hexokinase Method, ABACUS 3CP, ABACUS 5
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.
510(k) submissions have been managed by Ammirati Regulatory Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Diatron U.S., Inc.
3 devices