Duoject Medical Systems, Inc. is one of 195 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Duoject Medical Systems, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Duoject Medical Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bromont, Qc., CA.
Historical record: 3 cleared submissions from 2001 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Duoject Medical Systems, Inc. Filter by specialty or product code using the sidebar.
Duoject Medical Systems, Inc. — FDA 510(k) Products and Clearance History
3 devices
Cleared
Mar 13, 2014
E-Z LINK
General Hospital
164d
Cleared
Apr 02, 2008
SMART-ROD
General Hospital
398d
Cleared
Jun 25, 2001
INTER-VIAL
General Hospital
108d