Medical Device Manufacturer · US , Parisppany , NJ

Diagnostica-Stago - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2001
3
Total
3
Cleared
0
Denied

Diagnostica-Stago has 3 FDA 510(k) cleared medical devices. Based in Parisppany, US.

Historical record: 3 cleared submissions from 2001 to 2016. Primary specialty: Hematology.

Browse the FDA 510(k) cleared devices submitted by Diagnostica-Stago Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Diagnostica-Stago

3 devices
1-3 of 3
Cleared Dec 10, 2016
STA® - Liatest® D-Di
K162227 · DAP
Hematology · 124d
Cleared Sep 03, 2014
STA LIATEST D-DI
K141144 · DAP
Hematology · 124d
Cleared Jun 07, 2001
ROTACHROM HEPARIN AND STA -ROTACHROM HEPARIN
K010455 · KFF
Hematology · 129d
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