Medical Device Manufacturer · US , Lenexa , KS

Diatron U.S., Inc. - FDA 510(k) Cleared Devices

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

FDA 510(k) Regulatory Record - Diatron U.S., Inc. Hematology ✕

2 devices
1-2 of 2
Cleared Aug 02, 2012
ABACUS 3CP
K111534 · GKZ
Hematology · 427d
Cleared Mar 27, 2012
ABACUS 5
K112755 · GKZ
Hematology · 188d
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