Medical Device Manufacturer · US , Lenexa , KS

Diatron U.S., Inc.

3 submissions · 3 cleared · Since 2012
3
Total
3
Cleared
0
Denied

Diatron U.S., Inc. — FDA 510(k) Submissions

Diatron U.S., Inc. has submitted 3 FDA 510(k) premarket notifications since 2012, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Counter, Differential Cell, Hexokinase, Glucose . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
Filters
Filter by Specialty
All3 Hematology 2 Chemistry 1