Roche Diagnostics Corporation - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Roche Diagnostics Corporation has 6 FDA 510(k) cleared medical devices. Based in Indianpolis, US.
Historical record: 6 cleared submissions from 2007 to 2015. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Roche Diagnostics Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Roche Diagnostics Corporation
6 devices
Cleared
Mar 16, 2015
ACCU-CHEK CONNECT DIABETES MANAGEMENT APP
General Hospital
243d
Cleared
Dec 17, 2014
ACCU-CHEK AVIVA EXPERT SYSTEM
Chemistry
138d
Cleared
Apr 29, 2014
ACCU-CHEK AVIVA PLUS SYSTEM
Chemistry
131d
Cleared
Oct 18, 2011
ELECSYS T4 CALCHECK 5
Chemistry
48d
Cleared
Apr 17, 2007
AMPLICOR CT/NG TEST FOR NEISSERIA GONORRHOEAE
Microbiology
89d
Cleared
Apr 16, 2007
AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS
Microbiology
88d