NATROX TOPICAL OXYGEN DELIVERY SYSTEM WITH IODP
Jul 2012
298d
Inotec Amd , Ltd.
1
Total
1
Cleared
0
Denied
Inotec Amd , Ltd. — FDA 510(k) Submissions
Inotec Amd , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2012, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Chamber, Oxygen, Topical, Extremity . Use the specialty filter in the sidebar to narrow results.
1 devices