Dsrv, Inc. is one of 5140 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dsrv, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Dsrv, Inc. has 2 FDA 510(k) cleared medical devices. Based in Clarkston, US.
Historical record: 2 cleared submissions from 2014 to 2014. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Dsrv, Inc. Filter by specialty or product code using the sidebar.
Dsrv, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 10, 2014
REAGENT, RUSSEL VIPER VENOM - LA CONFIRM
Hematology
191d
Cleared
Jan 10, 2014
REAGENT, RUSSEL VIPER VENOM - LA SCREEN
Hematology
184d