ATAD ARD CATHETER
Jan 2005
315d
Atad Developments , Ltd.
1
Total
1
Cleared
0
Denied
Atad Developments , Ltd. — FDA 510(k) Submissions
Atad Developments , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2005, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Dilator, Cervical, Hygroscopic-laminaria . Use the specialty filter in the sidebar to narrow results.
1 devices